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Company:
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Joulé Clinical Staffing Solutions
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Booth:
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939
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Web:
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www.jouleclinical.com
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At Joulé Clinical Staffing Solutions you could say the right match
is in our DNA. For over 20 years, we've connected pharmaceutical,
biotechnology, clinical research and medical device clients to
professionals nationwide. Our specialized experience, geographic
reach and deep network enable us to provide the most qualified
clinical researchers, regulatory professionals and drug safety
specialists across the country. Recognized for providing superior
service, Joulé Clinical provides a complete range of staffing
solutions including contract, temporary, project and contract to
direct hire programs. The Right Match is in our DNA.
www.jouleclinical.com
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Company:
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Kansas Bioscience Authority
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Booth:
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200
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Web:
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www.kansasbioauthority.org
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The Kansas Bioscience Authority is a $581 million investment fund
that is advancing Kansas' national bioscience leadership by building
world-class research capacity; fostering the formation and growth of
bioscience startups; supporting expansion of the state's bioscience
clusters; and facilitating industrial expansion and attraction.
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Company:
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Kaplan EduNeering
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Booth:
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224
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Web:
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www.kaplaneduneering.com
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Kaplan EduNeering develops technology-enabled knowledge solutions
for assuring regulatory compliance, minimizing risk and improving
business performance. Clients around the world rely on our
cloud-computing learning solution that meets the regulatory
requirements within life science, energy, health plans, and general
industry.
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Kaplan EduNeering is a subsidiary of Kaplan Inc., a leading global
provider of educational services to individuals, schools and
businesses. Kaplan Inc. is a subsidiary of The Washington Post
company (NYSE: WPO).
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Company:
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Kayentis Inc
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Booth:
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322
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Web:
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www.kayentis.com
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Kayentis is the #1 publisher and operator of digital pen and smart
paper solutions for the healthcare industry. This solution based on
the Kayentis Digital Pen & Paper platform combine the best of the
physical and digital worlds: a very simple data collection method
(paper and pen) that offers the highest data accuracy, and all the
advantages of electronic management (real-time data, precise time
stamping, audit trail features, alerts).
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Kayentis is the sole Platinum Partner of Anoto qualified for its
core technology and its vertical solutions with a worldwide
capacity; thanks to the robustness of its platform and the quality
of its applications.
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Company:
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Kforce Clinical Research Inc.
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Booth:
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449
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Ticker Symbol & Exchange:
|
NASDAQ: KFRC (Kforce Inc.)
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Web:
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www.kforce.com/clinicalresearch
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Kforce Clinical Research provides customized, scalable outsourcing
solutions for clinical trials in the biopharmaceutical and medical
device industries. With more than 20 years experience in clinical
research, we collaborate with our clients to share our acquired
knowledge and leverage best practices to optimize clinical trial
execution and reduce cycle time. Our new proprietary technology
offers capacity management, forecasting and trending to help manage
the lifecycle of your trials. Every day we are Working At The Speed
Of Life - a guiding principle which holds us to a higher calling;
getting the life-changing medicines to those in need quickly,
without sacrificing quality.
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Company:
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Klein Hersh International
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Booth:
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403
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Web:
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www.kleinhersh.com
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Klein Hersh is your connection to the best and the brightest people
involved in the Life Sciences industry. We are immersed in all
aspects of the drug life cycle - touching everything from drug
discovery through clinical trials and commercialization with years
of deep industry expertise and a large, thriving network of
contacts. For over a decade we have placed over 400 Life Science
professionals each year. Whether your company needs a contract or
permanent staffing solution, we can help. We are uniquely positioned
as all of our Executive Search Consultants have individual desk
specialties, allowing a permanent and targeted presence in the
marketplace.
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Company:
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LabConnect, LLC
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Booth:
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641
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Web:
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www.labconnectllc.com
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LabConnect is a leading provider of central laboratory services to
the pharmaceutical industry. We offer both global central laboratory
services and a broad array of biomarker and specialized laboratory
support products. Our 30 locations across the globe offer our
clients a unique combination of geographic coverage and analytical
expertise that is unmatched in the industry today. To learn more
about LabConnect, please visit our website at www.labconnectllc.com
or contact us at 206.322.4680.
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Company:
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Laboratorio Hidalgo S.A.
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Booth:
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1556
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Web:
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www.laboratoriohidalgo.com
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Located in Buenos Aires, Argentina, Laboratorio Hidalgo provides
Central Laboratory Services related to the development of Clinical
Trials in South America: reliable results and an effective
logistics. The group is dedicated to meet the ever-changing demands
of today's market.
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Company:
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Langland
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Booth:
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1036
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Web:
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http://www.langland.co.uk/
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Langland is a leading full-service advertising agency, providing
communication strategies and execution specifically for the
healthcare sector. We are committed to developing integrated global
programs that accelerate the recruitment and maximize the retention
of patients for clinical trials.
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Langland is now the world's most creatively awarded healthcare
agency and ranked number one for creativity by the Institute of
Practitioners in Advertising. Our expertise has made a difference to
the success of over 100 clinical trials.
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Company:
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Liquent, Inc.
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Booth:
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248/250
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Web:
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www.liquent.com
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LIQUENT is the premier provider of a scalable, regulatory
information management platform and associated regulatory & clinical
services that can be leveraged throughout a client organization in
support of the development, registration, and manufacturing
processes. LIQUENT provides technology and outsourcing solutions
focused around regulatory submission preparation and tasks, dossier
planning, eCTD to CTD publishing and registration tracking
capabilities
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As a result, global life sciences companies, small tier to large
tier, rely on LIQUENT regulatory solutions to provide the technology
and services to compress the regulatory submissions and approval
process, improving speed to market, cost control, and productivity,
all of which contribute to ensuring patients' and physicians' timely
access to new drugs.
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Company:
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Logos Technologies Inc
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Booth:
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1441
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Web:
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www.logostechnologies.com
|
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ALPHADAS® is a world leading Early Phase EDC and Phase I site
automation system specifically designed for the complexities of
early phase clinical trials.
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Features include:
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• Schedule-driven & event based providing real-time, pro-active EDC
at the bedside, station or remote location.
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• Integrates with Sponsor Systems, medical devices, central ECG
systems and central laboratories minimising human data entry,
simultaneously reducing human error and increasing efficiency,
yielding immediate significant ROI
|
|
• Site specific tools provide workflow driven automation through
time driven, status based events plus bar-coded sample tracking,
further improving quality and traceability.
|
|
• Its depth of proven functionality over other systems to date has
been untouched
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Company:
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MAJARO InfoSystems, Inc.
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Booth:
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1006
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Web:
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http://www.majaro.com
|
|
MAJARO announces ClinAccess Prime™, the first eCRF solution
specifically designed for Phase I and other trials not suitable for
costly complex EDC systems.
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More than a decade after EDC's introduction, nearly 50% of all
trials are still conducted using paper CRFs. Sponsors often site
cost, lead time, and complexity as reasons for choosing paper over
EDC. ClinAccess Prime combines the benefits of EDC with the
simplicity and cost of paper. ClinAccess Prime transforms CRFs
created in Microsoft Word into electronic forms with extensive edit
check capabilities and the appearance of paper.
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MAJARO is the developer of ClinAccess, the leading SAS Powered®
clinical data management solution, that since 1987 has been used for
hundreds of clinical trials, over one million CRF pages, and
numerous successful drug, biologic, and medical device filings.
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Company:
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MaxisIT, Inc.
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Booth:
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734
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|
Web:
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www.maxisit.com
|
|
MaxisIT® offers Integrated Clinical Development Suite CTRenaissance®
and Clinical Functional Services to Pharmaceuticals and life
sciences companies and academia globally. CTRenaissance® helps
design, monitor, analyze, exchange and submit clinical trials data
and deliverables in a web-based environment on-demand.
CTRenaissance® is an integrated and affordable technology platform
that helps reduce cycle time; and empowers business users to
prospectively plan, monitor & optimize next generation clinical
trials in a more predictable, controlled and regulatory compliant
environment that can span across geographical boundaries - enabling
the key priorities and core research managed intelligently and
confidently. Visit us at booth number 734 and learn more.
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Company:
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McGuire Research Institute
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Booth:
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1557
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|
McGuire Research Institute (MRI) is a clinical research site located
in the Richmond VA Medical Center. We conduct Phase 1-4 outpatient
and inpatient studies. Areas of strength are diabetes/lipids,
cardiovascular, pulmonary, infectious disease, Hep C, Crohn's, liver
disease, prostate disease, geriatrics, Parkinson's and traumatic
brain injury. MRI was incorporated in 1989 and has received over 100
million in direct support primarily from the pharmaceutical industry.
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Company:
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MedAssurant, Inc
|
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Booth:
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662
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|
Web:
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www.medassurant.com
|
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MedAssurant focuses on the analysis of huge healthcare data sets to
drive dramatic, quantifiable improvements in clinical and quality
outcomes. MedAssurant's MORE2 Registry is a comprehensive dataset
covering 70 million Americans with over 4.8 billion medical events
to drive CER, pre/post-marketing activities and pharmacosurveillance
programs.
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Company:
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MedNet Solutions
|
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Booth:
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425
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|
Web:
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www.mednetstudy.com
|
|
MedNet Solutions is a leading healthcare technology company
specializing in electronic data capture (EDC) and clinical study
management systems designed for the global life sciences market.
Applying critical insight, proven technology and unwavering support,
MedNet delivers powerful, flexible and easy-to-use web-based
eClinical solutions that support our customers' clinical studies,
registries and investigator initiated trials. Since 2000, MedNet has
successfully supported leading pharmaceutical, medical device,
biotechnology, and clinical research organizations on projects
spanning 6 continents and more than 40 countries. MedNet delivers a
superior customer experience from beginning to end. For more
information, please visit www.mednetstudy.com.
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Company:
|
META Solutions
|
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Booth:
|
1340
|
|
Web:
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www.metasol.com
|
|
META Solutions, Inc. is a regulatory compliance consultancy with
over 20 years of experience assisting over 250 biopharmaceutical and
related service companies to managing their regulatory compliance
risk by assessing non-compliance, and then developing and
implementing practical solutions, with expert guidance and training.
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Company:
|
MidLands IRB, LLC (MLIRB)
|
|
Web:
|
www.mlirb.com
|
|
Founded in 1981, MLIRB is an AAHRPP fully-accredited Independent
Review Board. Focusing on protecting the rights and welfare of
research study participants, MLIRB specializes in providing
customized, personalized, and responsive services to its client
partners. MLIRB provides IRB review for clients nationwide, for all
phases of research, and in all therapeutic areas. MLIRB has
extensive experience in multi-site trials, with two Boards that meet
weekly. MLIRB also offers custom consent development services, and
our FDA audit history is clear - no 438 ever issued.
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Company:
|
MIR- Medical International Research USA
|
|
Web:
|
www.spirometry.com
|
|
MIR is a dynamic company which develops and manufactures
spirometers, telemedicine and oximeters at reasonable costs. MIR
sells its spirometry, tele-spirometry and oximters devices
worldwide. Given the extensive in-house know-how, the company
develops and produces innovative devices, software plus solutions
for telemedicine applications.
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Our products enjoy an unrivalled reputation for accuracy and product
reliability both amongst lung function specialists and university
professors and other opinion leaders worldwide. MIR has a wide
international presence: our products are sold in more than 70
countries. Our USA office which provides sales, service and support
for the USA is based in Milwaukee WI.
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Company:
|
Mission3, Inc.
|
|
Booth:
|
151
|
|
Web:
|
www.mission3.com
|
|
Mission3 is the premier Regulatory Information Management software
company for the Life Sciences industry. Mission3's solution includes
electronic document management solutions for managing regulatory,
clinical and corporate documents; Virtual Data Rooms to securely
manage the due-diligence process for M&A and partnerships; full
regulatory submission management that includes support for eCTD,
510(k), PMA, and paper/electronic publishing to compliment
submission and dossier management. Topping off this extensive list
of solutions to the Life Science industry is Mission3 GlobalTrack, a
business intelligence platform that provides companies increase
visibility into their global regulatory initiatives. All Mission3
solutions are 21 CFR Part 11 compliant.
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Company:
|
Myoderm
|
|
Booth:
|
704
|
|
Web:
|
www.myoderm.com
|
|
Myoderm is a leading service provider for global procurement of
commercial pharmaceuticals including drugs utilized for comparator,
rescue, adjunctive or concomitant therapy. We utilize our
experience, knowledge, supplier and manufacturer network to provide
clients with critical information and accurate delivery of product.
In addition, Myoderm can act as the Central Depot for direct to
clinical site distribution as an alternative to local site sourcing
and ensure standardization of medications across your clinical sites.
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Company:
|
National Death Index
|
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Booth:
|
2012
|
|
Web:
|
http://www.cdc.gov/nchs/ndi.htm
|
|
The National Death Index (NDI) is a central computerized index of
death record information on file in the state vital statistics
offices. Working with these states, NCHS established the NDI as a
resource to aid epidemiologists and other health and medical
investigators with their mortality ascertainment activities.
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Company:
|
NeuroVive Pharmaceutical
|
|
Booth:
|
4425
|
|
Ticker Symbol & Exchange:
|
NVP (Sweden: AktieTorget)
|
|
Web:
|
www.neurovive.com
|
|
NeuroVive Pharmaceutical is a Swedish drug development company whose
primary mission is to conduct research and develop pharmaceuticals
that protect nerve, cardiac and other cells undergoing
health-threatening traumas or ischemia. In addition to conducting or
supporting clinical trials of NeuroSTAT® for traumatic brain
injuries and CicloMulsion™ to protect cardiac tissue during
myocardial infarction, NeuroVive is researching and developing
variants of cyclophilin-D-inhibiting cyclosporins and new ways of
transporting these drugs across the blood-brain barrier to the CNS.
NeuroSTAT® is in a Phase II/III (adaptive) clinical study while
CicloMulsion™'s efficacy is being examined in a 1000-person Phase
III investigator-initiated study.
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Company:
|
NewCardio, Inc
|
|
Booth:
|
1660
|
|
Ticker Symbol & Exchange:
|
NWCI.OB
|
|
Web:
|
www.newcardio.com
|
|
Newcardio is a cardiovascular diagnostics company that offers
QTinno, 3D technology to significantly increase the value of the
standard ECG for cardiac toxicity analysis in clinical studies.
QTinno automates ECG processing -the selection, measurement and
analysis of ECGs - to provide superior data accuracy over standard
semi-automated methods. QTinno can dramatically reduce study costs
while providing increased precision to allow studies to be run with
fewer subjects while retaining statistically significant study power.
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Company:
|
New Orleans Center for Clinical Research
|
|
Booth:
|
1515
|
|
Web:
|
www.noccr.com
|
|
NOCCR and VRG are privately owned multispecialty clinical research
groups dedicated to advancing medicine by evaluating investigational
drugs and devices. The companies share two primary missions of equal
importance: to help develop safe, advanced medical options in an
ethical manner and to deliver high-quality, clean data to our
sponsors. We have conducted over 1500 clinical trials in the last 25
years. With combined space exceeding 23,500 sq. ft., full-time MDs,
Nurse Practitioner, Nurse/Coordinators, EMTs, nursing assistants,
and separate regulatory, data and recruiting departments, we have
earned a reputation for excellence and consistently exceeding
enrollment goals.
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Company:
|
NextDocs
|
|
Booth:
|
717
|
|
Web:
|
www.nextdocs.com
|
|
NextDocs is the worldwide leader in providing Microsoft
SharePoint-based document and quality management solutions to life
sciences organizations. It enables businesses in regulated
industries to achieve compliance with FDA and other agencies while
automating processes, improving efficiency and dramatically reducing
costs. The NextDocs Global Alliance Program connects our clients
with market-leading software and service providers to deliver the
most robust suite of enterprise content management and quality
management software and delivery solutions.
|
|
|
|
|
NextDocs has earned the ISO 9001:2008 certification which is
recognized internationally and in the most comprehensive standard in
the ISO 9000 series.
|
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|
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Company:
|
Next Generation Clinical Research
|
|
Booth:
|
539
|
|
Web:
|
www.nextgenclinical.com
|
|
Next Generation Clinical Research is a CRO providing clinical trial
management services in pharmaceutical, biologic, medical device and
diagnostic product development with a focus on collaborations with
emerging and small to mid-size companies. Although we have
experience in a variety of therapeutic areas, we command particular
expertise in critical care, nephrology and central nervous system
disorders as well as specialize in complex projects and innovative
product applications. Our services include strategy, project
management, investigator identification, clinical monitoring,
medical safety, data management and reporting.
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Company:
|
Norwich
|
|
Booth:
|
556
|
|
Web:
|
www.norwichpharma.com
|
|
Norwich is a recognized leader and single-source provider in
full-service contract pharmaceutical development and manufacturing,
offering R&D, GMP pilot scale manufacturing, analytical development
and validation, and testing services. A full range of manufacturing
and packaging capabilities and resources includes non-potent and
intermediate potency tablet and capsule solid dose forms, and
semi-solid and liquid dose forms. Norwich also combines
comprehensive services and customer focus to offer a complete range
of clinical services, including pharmacovigilance, bioanalytical
services and clinical research programs. Founded upon a reputation
for quality, compliance and dependability over 100 years ago,
Norwich strives to deliver uncommon value and everyday excellence to
its customers.
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Company:
|
Nova Language Services
|
|
Booth:
|
135
|
|
Web:
|
www.nova-transnet.com
|
|
NOVA is a well respected provider of multilingual language
services to the CRO/Regulatory affairs sectors. From clinical
trial protocols to marketing authorisation dossiers, we will
fulfill all your translation requirements with expertise, accuracy
and reliability in all European languages. NOVA is ISO 9001:2008
and UNE EN 15038 certified. Nova has been included in the top ten
translation providers in Southern Europe by Common sense advisory.
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Company:
|
Novella Clinical
|
|
Booth:
|
1529
|
|
Web:
|
www.novellaclinical.com
|
|
Novella Clinical, Inc. is a full service contract research
organization headquartered in Research Triangle Park, N.C. For more
than a decade, Novella has served as an active partner to the
oncology, biopharma and medical device industries. As the first
global eCRO, Novella integrates deep clinical expertise with
industry-leading technologies and a proven approach to support,
streamline and expertly resource the entire product development
process.
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Company:
|
nSpire Health
|
|
Booth:
|
914
|
|
Web:
|
www.nspirehealth.com
|
|
nSpire Health supplies pharmaceutical companies, CROs, & clinical
researchers advanced technology, precise instrumentation, & expert
professional services to accelerate respiratory clinical trials
worldwide. We continue to redefine accuracy and establish new
standards for diagnosing, treating, & managing lung disease;
delivering the shortest path to data lock.
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Company:
|
Online Business Applications
|
|
Booth:
|
1942 and 1944
|
|
Web:
|
www.irmsonline.com
|
|
For over twenty five years, Online Business Applications has been
committed to providing advanced software solutions for the
Pharmaceutical, Biotechnology, and Medical Device industries in the
areas of Medical Communications and Drug Safety. We utilize proven
leading-edge technologies, anticipate our clients' needs, and
deliver solutions that exceed expectations, making us the medical
communications software provider of choice.
|
|
|
|
|
Engineered in partnership with over 100 pharmaceutical and biotech
companies, IRMS has extensive off-the-shelf functionality. The
outstanding scalability and power of IRMS has allowed us to
establish ourselves as the market leader in medical communications
systems.
|
|
|
|
|
OBA has successfully provided global medical information solutions
which have been deployed to clients in over 70 countries.
|
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Company:
|
OptumInsight
|
|
Booth:
|
1945 & 2045
|
|
Web:
|
www.optum.com
|
|
OptumInsight™ is part of Optum™, a leading health services business
dedicated to making the health system work better for everyone.
OptumInsight builds on the legacy of such industry leaders as
QualityMetric, CanReg, Innovus, HTanalysts, ChinaGate, and Ingenix
to save lives, improve care, and transform health communities by
offering analytics, technology, and consulting services that enable
better decisions and results. OptumInsight partners with clients
across the health system-including health plans, physicians,
hospitals, life sciences companies, and government agencies-to
provide solutions that meet their unique needs through flexible
delivery models. For more information, visit www.optum.com.
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Company:
|
Orlando Clinical Research Center
|
|
Booth:
|
1328
|
|
Web:
|
www.ocrc.net
|
|
Orlando Clinical Research Center is an independent Phase I-IV
custom-built 35,000 sq. ft. research site designed for Phase 1
clinical trials located in the heart of Central Florida. Facility
includes 110 in-house volunteer beds, dual lead digital telemetry,
CCTV security system, and cardkey access. A special
treatment/observation area has 12 hospital beds (6 used for onsite
Hemodialysis studies). OCRC is specialized in Phase 1 - 4 trials
with an emphasis in pharmacokinetic studies in healthy, hepatic,
hemodialysis and renal populations.
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Company:
|
Outcome
|
|
Booth:
|
1302
|
|
Web:
|
www.outcome.com
|
|
Outcome is a global, scientific and operationally based company
focused exclusively on evaluating real-world safety and
effectiveness outcomes through registries, studies, data and
technologies. Backed by expertise and experience in more than 40
therapeutic areas, our teams have designed and implemented an
industry-leading number of patient registries including many of
the largest and most well-recognized programs for disease
outcomes, safety and risk management, and effectiveness, across 90
countries. Our teams have led landmark initiatives, including the
development of the patient registries guidebook for AHRQ, the
GRACE Principles, and the US government-sponsored Registry of
Patient Registries (RoPR) (in development). Outcome is an AHRQ
DEcIDE Research Center and an EMA PROTECT-EU partner and ENCePP
research center. We have offices in North America, Europe, and
Asia.
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Company:
|
Palm Beach CRO
|
|
Booth:
|
535
|
|
Web:
|
www.PalmBeachCRO.com
|
|
Palm Beach CRO provides clinical services that meet the highest
quality standards with appropriate client timelines. PBCRO manages
the entire clinical trial process from site selection, investigator
meetings, monitoring, IRB, regulatory affairs, data management,
statistical analysis and final reports of multi-center trials
throughout the USA
|
|
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Company:
|
Paragon Biomedical
|
|
Booth:
|
1928 and 1930
|
|
Web:
|
www.paragonbiomedical.com
|
|
Paragon Biomedical is a global, full-service contract research
organization (CRO) providing high quality Phase I-IV clinical trial
support to biopharmaceutical and medical device companies, with
proven capabilities and expertise in major therapeutic areas.
Paragon's unique corporate culture attracts the industry's top
associates who share a strong commitment to excellence and vision in
the passionate pursuit of better healthcare through integrity,
teamwork, diversity, and life balance. Paragon is a certified
woman-owned business with <20% staff turnover rate in last 4 years;
88% repeat business rate; 6-8 week rapid start-up; and 93% of
studies on or ahead of targeted enrollment.
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Company:
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PAREXEL International
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Booth:
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1623
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Ticker Symbol & Exchange:
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PRXL
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Web:
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www.PAREXEL.com
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PAREXEL, a leading global biopharmaceutical services provider,
complements client organizations with strategic insight, in-depth
scientific knowledge, tactical expertise and a wealth of experience
throughout the product development process. The Company provides
worldwide regulatory expertise, Phase I - IV clinical research
services, and eClinical technologies that accelerate development, as
well as reimbursement and market access services. PAREXEL provides
the right guidance and high levels of quality needed to accelerate
development and commercialization. Operating 71 locations throughout
52 countries, PAREXEL has the right experts in the right
geographical locations for any aspect of designing and executing
regional and global clinical development programs.
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Company:
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PCM TRIALS
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Booth:
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157
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Web:
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PCMTRIALS.com
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PCM TRIALS own Certified Mobile Research Nurses (CMRN) understand
the complex and unique requirements of mobile clinical trial
research. CMRNs are hired, screened, trained and managed by PCM
TRIALS (not a third party agency) and have completed more than 4,300
mobile clinical trial visits across the U.S. in a wide variety of
therapeutic areas.
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Utilizing PCM TRIALS' CMRNs, you can improve recruitment and
retention, accelerate your trial, lower your risk by getting the
same quality and services as on-site visits, obtain clean source
data and access PCM TRIALS own certified mobile research nurses
nationwide with partners in Canada and overseas.
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Company:
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PDR Network, LLC
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Booth:
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202-204
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Web:
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PDRnetwork.com
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PDR® Network - the industry's #1 source for trusted drug
information. An industry partner for over 65 years, PDR Network
plays a crucial role in providing critical drug information to
prescribers within their workflow. Since our first Physicians' Desk
Reference® (PDR®), we have evolved to meet the industry's changing
needs. Today, the PDR is distributed to nearly 500,000 U.S.
prescribers and used over 70M times annually. Our products deliver
that content via PDR.net®, mobilePDR®, PDR®3D™ and EHR platforms.
Visit booth 202 for a demonstration of RxEvent and see how we are
changing adverse event reporting, turning lemons into lemonade for
manufacturers.
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Company:
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Pharmaceutical Outsourcing
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Booth:
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111
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Web:
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http://pharmoutsourcing.com
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Pharmaceutical Outsourcing, the journal dedicated to pharmaceutical
and biopharmaceutical contract services. With regular sections on
contract manufacturing, contract research, contract packaging,
formulation/development services, contract analytical testing, APIs,
stability testing, clinical research and other areas, we bring the
most complete coverage of trends and issues in the industry to our
15,000 readers in North America.
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Company:
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Pharmaceutical Safety Services
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Booth:
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2057
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Web:
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PharmSafetyServ.com
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Pharmaceutical Safety Services, LLC, is dedicated to provide a
complete range of services to pharmaceutical, biotech, device
companies, and contract research organizations to develop and
implement safety and adjudication boards in the conduct of clinical
research programs.
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Pharmaceutical Safety Services, LLC, and all safety and adjudication
board members are independent of any study and sponsor in which we
are involved in all regards including:
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• Participation in the study conduct
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• Any financial interest in the study, clinical program or sponsor
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• Any potential financial or publication interest in the study
outcome
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Phone (855-856-2500)
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www.PharmSafetyServ.com
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5776 Ruffin Road
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San Diego, CA 920
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Company:
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PharmaNet
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Booth:
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1655
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Web:
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www.pharmanet.com
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PharmaNet Development Group, a recognized leader of global drug
development services to the pharmaceutical, biotechnology, generic
drug, and medical device industries, provides comprehensive
capabilities in Phase I-IV clinical development, bioanalytical and
bioequivalence services, regulatory, staffing, and therapeutic
solutions. For the applied knowledge and intelligent solutions
needed to accelerate drug development programs of all sizes around
the world, PharmaNet works for you.
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Company:
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PharmaVigilant
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Booth:
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255
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Web:
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www.pharmavigilant.com
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PharmaVigilant is a SaaS company providing a fully integrated
solution for clinical development. Our suite of patient-based
software and services automate the collection, management and
analysis of clinical trial data. Sponsors rely on us to ease the
regulatory and FDA submission and approval process and ultimately
go-to market more quickly with top quality drugs. We offer a full
suite of clinical trial technology offerings including Electronic
Data Capture (InSpire EDC), Study Building (I-Builder), Electronic
Trial Master File System (I-Vault eTMF), Automated Site Payment
System (PaySite), Remote Source Document Verification (I-Vault
rSDV), Study administration (InSpire Control Center) and Data
Warehousing (I-Warehouse).
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Company:
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PharmaVOICE
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Booth:
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1423
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Web:
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www.pharmavoice.com
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PharmaVOICE magazine, reaching more than 25,000 BPA-qualified
life-sciences executives, is the forum that allows business leaders
to engage in a candid dialogue on the challenges and trends
impacting the industry. PharmaVOICE provides readers with insightful
and thought-provoking commentary in a multiple-perspective format
through forums, topics, and articles covering a range of issues from
molecule through market. PharmaVOICE subscribers are also kept
abreast of the latest trends and information through additional
media resources, including WebLinx Interactive WebSeminars,
Podcasts, Videocasts, White Papers, E-Surveys and e-Alerts.
Additionally, PharmaVOICEMarketplace.com provides a comprehensive
directory of products, services, and solutions for the life-sciences
industry.
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To Raise Your VOICE, contact [email protected].
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Company:
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Pharm-Olam International
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Booth:
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1227
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With 27 offices among the world's most populated cities, Pharm-Olam
International provides cost effective coverage in both emerging and
traditional markets for Phase I to IV clinical studies. Since 1994
we have used our local knowledge of an investigator's past
performance, competing studies, and regulatory environment to offer
sponsors an accurate and informed plan to complete trials on time.
We provide full service and strategic outsourcing across all
therapeutic areas. Contact Pharm-Olam for a complimentary
feasibility study for your next clinical trial.
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Company:
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Philips Respironics
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Booth:
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457
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Web:
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www.ribn.respironics.com
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Philips is a global leader in heath and well being. This position
has been achieved by understanding the needs of our customers and
delivering innovative, products that live up to our brand promise of
Sense and Simplicity.
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Come to booth 457 and learn how Actiwatch can help you in your
upcoming trials.
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Company:
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Phlexglobal Limited
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Booth:
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222
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|
Web:
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www.phlexglobal.com
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Established in 1997 Phlexglobal is a specialist global Contract
Research Organization with a unique combination of clinical trial
knowledge, document management skills, regulatory understanding and
technical expertise. Experts in paper and electronic Trial Master
Files with a unique solution PhlexEview enabling centralized viewing
of documentation.
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Company:
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PHT Corporation
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Booth:
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1612/1613
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|
Web:
|
www.phtcorp.com
|
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PHT is the global innovator and experience leader in ePRO
(electronic patient-reported outcome) Systems that reduce costs and
improve data quality in clinical trials and post marketing studies.
Since 1994, patient experiences captured by PHT's ePRO System have
been used successfully in over 465 global trials by more than 100
biopharmaceutical companies, resulting in at least 19 regulatory
submissions and 16 approvals to date. The benefits ePRO systems
provide to sponsors include reliable patient compliance; reduced
data variance of PRO endpoints for smaller, more conclusive trials;
increased patient safety monitoring; and, decreased timelines from
trial end to data analysis. Sponsors using PHT's ePRO System
consistently report significant R&D cost savings and better
scientific outcomes vs. paper.
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Company:
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Phoenix Software International
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Booth:
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1348
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Web:
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www.phoenixsoftware.com
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Phoenix Software International® presents Entrypoint Plus®, a
complete system for creating, deploying, and administering custom
electronic data capture applications for clinical trials. Entrypoint
is built around a scalable, client-server network architecture using
ODBC to interface with SQL databases. EPX™ is a new product that
offers the features of Entrypoint Plus for the web browser. Deploy
your applications on a web server and create batches that can be
accessed by any computer with a web browser and Internet access.
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Company:
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PleaseTech Ltd
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Booth:
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1243
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Web:
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http://www.pleasetech.com/
|
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PleaseTech Ltd specializes in software solutions for the document
review and co-authoring process.
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|
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PleaseTech's flagship product, PleaseReview™, is a collaborative
review and co-authoring solution for Microsoft Word and other
document types. PleaseReview facilitates secure, simultaneous
collaboration across the organization and externally with third
parties within a secure, controlled environment. It is therefore
ideally positioned for use by Medical Writing, Regulatory, Clinical,
Quality and other departments within the Life Sciences sector.
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In addition to PleaseReview's unique collaborative review
environment, it offers full management and control over the
document, comment and change reconciliation, comprehensive reporting
and is available integrated with leading DMS.
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Company:
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Premier Research Group Limited
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Booth:
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311
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|
Web:
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http://www.premier-research.com
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|
Premier Research is a professional services company providing
clinical development support to biopharmaceutical and medical device
industries. Founded in 1989 and headquartered in Philadelphia, the
company has 22 offices across North America and Europe and operates
in over 30 countries worldwide. The company is a leader in
performing research in analgesia, oncology, pediatrics, medical
devices and neurosciences. Additionally, it has a strong strategic
sourcing group that supports resource planning and management.
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The company offers comprehensive services for every phase of
development including, regulatory affairs, clinical trial
management, medical affairs and consulting, pharmacovigilance, data
operations, biostatistics, medical writing, IVRS/IWRS, and quality
assurance.
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Company:
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Pretium
|
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Booth:
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1463
|
|
Web:
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www.pretium.com.au
|
|
Pretium is an Australian-owned, outsourcing organization that
supports your research efforts from study design through to
publication. We design and implement programs to undertake phase III
and IV clinical research, utilizing strong alliances with primary
care networks we deliver rapid investigator and patient recruitment,
and coordinated management. Our primary care network and study
coordinators provide a unique opportunity to conduct large phase III
and IV trials efficiently. In addition, Pretium staff has experience
working across a wide range of therapeutic areas. We can work with
the key opinion leaders you select, or use our expertise and
feasibility process to select investigators suitable for your
project.
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Company:
|
Projecis, Inc.
|
|
Booth:
|
511
|
|
Web:
|
www.projecis.com
|
|
Projecis, a knowledge convergence platform, enables project
stakeholders to easily connect teams, organize data, and disseminate
information for better business decision-making. Users can access
project status, time measures, files, data, issues, member profiles
(including LinkedIn®) - even informative videos with interactive
transcripts - via this secure, web-based platform. Team exchange is
enhanced with Communication 2.0 features with options for connecting
with members using Skype®, VoIP calls, email integration, text
alerts, and real-time discussions & commenting.
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Company:
|
PRUDENTAS
|
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Booth:
|
363
|
|
Web:
|
www.prudentas.com
|
|
PRUDENTAS is a Contract Research Organization, which offers to
pharmaceutical and biotech companies comprehensive set of services
and experienced team for Phase I - IV clinical trials conducted in
Russia and Ukraine with fast recruitment and uncompromised high
quality. PRUDENTAS offers the following services for Phase I - IV
trials in Russia and Ukraine: Study documents preparation,
Regulatory support of the study, Clinical trial monitoring, GCP
Auditing, preparation for regulatory inspection, audits support, GCP
training for investigators, Site Management, Project Management.
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Company:
|
Quality Associates, Inc.
|
|
Booth:
|
517
|
|
Web:
|
www.qualityassociatesinc.com
|
|
Quality Associates, Inc. (QAI) was established in 1986 to provide
Quality Assurance (QA) consulting services to the pharmaceutical and
agrochemical industries.
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|
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|
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QAI's large staff of Quality Assurance professionals have practiced
as scientists in regulated industries before joining QAI, including
monitoring clinical studies and making regulatory submissions to
FDA. Our auditors therefore conduct quality assurance functions
under GLP and GCP with an understanding of the science and the
regulations governing the studies reviewed. Several have been
accepted as RQAP-GLP.
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|
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QAI's corporate office are located between Washington, DC and
Baltimore, MD. QAI maintains additional offices in several other US
locations.
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Company:
|
Queensland Clinical Trials Network Inc.
|
|
Booth:
|
600
|
|
Web:
|
www.qctn.com.au
|
|
QCTN is an independent, Australian-based, not-for-profit
organisation.
|
|
|
|
|
As a peak industry association, QCTN is an 'umbrella organisation'
representing more than 100 businesses that have a presence in
Queensland. These organisations are life sciences service providers
and related entities serving the pharmaceutical, biotechnology,
complementary medicines and medical devices industries.
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|
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|
|
As a primary point of contact for international organisations
seeking to undertake (pre)clinical drug development in Australia,
QCTN helps identify and connect overseas organisations with
appropriate Australian research institutes, biotechnology and
medical device companies and life sciences service providers.
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|
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|
|
QCTN is involved in organising trade missions, industry workshops,
conferences, government advocacy, establishing and maintaining
relationships with other industry groups around the world.
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Company:
|
RANDOX PHARMA SERVICES
|
|
Booth:
|
305
|
|
Web:
|
www.randoxpharmaservices.com
|
|
Randox has been providing solutions to world-class research and
diagnostic establishments for 30 years and is committed to producing
world class testing technology for human diseases.
|
|
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|
|
We have unrivalled in-house technical know-how in the development of
biomarker assays, companion diagnostics and life science materials
as well as the inception of our award winning Biochip Array
Technology which allows simultaneous detection of multiple proteins
and genes in a single sample, with arrays developed specifically for
clinical and research settings.
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|
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|
|
The RX Series of clinical chemistry analyzers offer over 120 assays
and provide quality results at every phase. We also offer a full
range of Quality Control products and unique customizable services
in each area.
|
|
|
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|
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Company:
|
R&D Directions (UBM Canon)
|
|
Booth:
|
1104
|
|
Web:
|
www.pharmalive.com
|
|
R&D Directions provides insight into pharmaceutical research and
development, from discovery through clinical trials and submission.
Leaving the hard science to other publications, R&D Directions
focuses on pharmaceutical companies' R&D business strategies and
decisions. Editorial content covers drugs, therapeutic categories,
industry segments, and strategies, and imparts extensive
intelligence on products in the pipeline. Although R&D Directions
contains a wealth of medical and scientific information, it is
written in a non-clinical, non-technical style. For more
information, visit www.pharmalive.com or email [email protected]
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|
Company:
|
ResearchPoint
|
|
Booth:
|
1714
|
|
Web:
|
www.researchpoint.com
|
|
ResearchPoint is a full-service global CRO with proven expertise in
supporting clinical trials for pharmaceutical, biotechnology and
medical device companies. With expertise spanning all major
therapeutic areas, ResearchPoint delivers a unique blend of an
experienced team, combined with the creativity, responsiveness, and
customer-focus of a highly nimble organization. ResearchPoint
approaches every clinical project with a focus on problem-solving
and foresight. Beginning from the proposal stage with our rigorous
risk mitigation planning and precise preparation, to delivery of the
final report, the company strives to surpass every client's
expectation.
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Company:
|
Rho
|
|
Booth:
|
301
|
|
Web:
|
www.rhoworld.com
|
|
Rho is a full service CRO dedicated to enhancing the quality and
speed of its customers' clinical trials through the highest levels
of performance, accuracy, and scientific integrity. Rho contributes
to the success of pharmaceutical, medical device, and biotechnology
studies in a range of therapeutic areas.
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Company:
|
RxLogix Corporation
|
|
Booth:
|
1764 and 1766
|
|
Web:
|
www.rxlogix.com
|
|
RxLogix is the foremost provider of business and technology services
for Safety and Pharmacovigilance. Our team of experts has spent many
years focusing in this domain and brings experience of best
practices across all areas. RxLogix Solutions have been developed by
the leading experts on the Oracle Argus Safety suite and Drug Safety
. Business: we understand the challenges and will advise, mentor and
lead the change process in your organization. Technology: we work
with the industry-leading databases and our solutions will allow you
to implement, upgrade and validate your systems faster and at lower
cost. RxLogix delivers results everytime.
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Company:
|
RWD Technologies, a Division of GP
|
|
Booth:
|
2009
|
|
Ticker Symbol & Exchange:
|
NYSE: GPX
|
|
Web:
|
www.rwd.com
|
|
RWD's focus is to assist its global clients operationalize their
business strategies and transform their knowledge workers. By taking
a holistic view of initiative success that includes work processes,
organizational environment, skills and knowledge, and systems and
tools, our clients realize a significant shift in worker
performance. In the pharmaceutical industry, RWD's infoMaestro™
solution enables rapid access and delivery of Regulated or
Time-Sensitive Information across an enterprise, allowing for quick
implementation and integration while avoiding the costly bottlenecks
associated with custom solutions. Employees can better author,
manage, and distribute information for maximum productivity.
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Company:
|
SAS Institute Inc
|
|
Booth:
|
1349
|
|
Web:
|
www.sas.com/dia
|
|
SAS is the leader in business analytics software. For 34 years, SAS®
has helped the life sciences industry accurately analyze research,
clinical and business data. SAS is the industry standard and choice
for 100 percent of biopharmaceutical companies on the FORTUNE Global
500®. Since 1976, SAS has given customers THE POWER TO KNOW®.
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Company:
|
Schlafender Hase GmbH
|
|
Booth:
|
1363
|
|
Web:
|
www.schlafenderhase.de
|
|
If you don't like to proofread you will love TVT. The Text
Verification Tool (TVT) developed by Schlafender Hase is the global
standard in computer-driven proofreading. It helps save time, money,
improve quality, and avoid embarrassment and legal costs that can
result from avoidable mistakes. Easy to use, quick, accurate, ISO
certified for Design and Software Development for Regulated
Environments (ISO 9001), 21CFR Part 11 compliant, especially suited
for SPL. TVT - more proof and less reading.
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|
Company:
|
SGS Life Science Services
|
|
Booth:
|
1309
|
|
Ticker Symbol & Exchange:
|
SGSN
|
|
Web:
|
www.sgs.com/LifeScience
|
|
SGS Life Science Services is a leading contract service organization
providing clinical research services, analytical development,
biologics characterization, and quality control testing. We serve a
variety of companies including pharmaceutical, biopharmaceutical,
biotechnology and medical device manufacturers. SGS provides
clinical trial management (Phase I to IV) and services encompassing
data management, statistics and regulatory consultancy. Our
laboratory services include bioanalytical and immunogenicity
testing, analytical chemistry, microbiology, stability studies, and
extractables and leachables. With the acquisition of M-Scan, SGS
extends it service expertise in protein/glycoprotein
biopharmaceutical characterization using high-end mass spectrometry.
|
|
|
|
|
SGS Life Science Services is a truly global organization with 1,300
employees, located in 25 facilities, in 14 countries.
|
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Company:
|
Small Planet Events Inc
|
|
Booth:
|
1457
|
|
Web:
|
www.smallplanetevents.com
|
|
Small Planet Meetings provides you a specialised, first class event
management service delivering creative and cost effective solutions
for the pharmaceutical industry.
|
|
|
|
|
We work with you from the start, planning an event that delivers
your goals and creates a lasting memory for all your attendees long
after the event has finished.
|
|
|
|
|
We have over 15 years experience within event management; our
expertise and focus on service has won us contracts in all corners
of the earth. Such events include investigator meetings, internal
sales conferences, advisory boards, KOL and Steering Committee
meetings.
|
|
|
|
|
An experienced event planner required? Give us a call!
|
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|
|
|
|
|
|
Company:
|
Soltex Consulting
|
|
Booth:
|
1015
|
|
Web:
|
www.soltexconsulting.com
|
|
Soltex Consulting is a privately held, independent consulting firm
that advises our clients on driving efficiencies throughout the
clinical trial lifecycle. Soltex employs an innovative framework to
analyze business problems-examining them through the lens of People,
Processes and Technology. We then recommend value-driven strategies
and implement solutions to tackle our clients' most critical issues.
|
|
|
|
|
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|
|
Company:
|
Sonic Clinical Trials
|
|
Booth:
|
1459
|
|
Web:
|
www.sonicclinicaltrials.com
|
|
Sonic Clinical Trials is a dedicated central laboratory service
providing comprehensive clinical trials support to the
pharmaceutical and biotechnology industries in the Asia-Pac region.
Our central laboratory provides a superior service exclusively in
support of clinical trials and we aim to meet each client's unique
requirements for their study by offering flexible service options,
high quality results and project management.
|
|
|
|
|
SCT is committed to the maintenance of uncompromising ethical
standards in all our business and medical interactions. Our
laboratory has been able to develop its systems and services, over
the years, to match its growth and remain at the cutting edge of
pathology technology, logistics and efficiency.
|
|
|
|
|
Our laboratory is fully accredited by the National Association of
Testing Authorities and is committed to maintaining the highest
technical & professional standards.
|
|
|
|
|
|
|
|
Company:
|
Spaudling Clinical LLC
|
|
Booth:
|
1905
|
|
Web:
|
www.spauldingclinical.com
|
|
Spaulding Clinical Research, LLC (www.spauldingclinical.com) is a
Clinical Pharmacology Research Unit and Cardiac Core Lab that offers
a full range of global services from study design through study
execution/conduct, data management, statistical analysis, and
clinical summary/expert reporting. Spaulding has extensive
experience conducting TQT, first-in-human, multiple rising dose,
bioavailability/bioequivalence, drug interaction, and food effect
studies. Spaulding offers the complete suite of services for
centralized ECG studies, including the proprietary Spaulding IQ
electrocardiograph, designed to provide data that is twice as good
at half the cost and fits in the palm of your hand!
|
|
|
|
|
|
|
|
Company:
|
Spectra Clinical Research
|
|
Booth:
|
1822
|
|
Web:
|
www.spectraclinicalresearch.com
|
|
As a global provider of central laboratory services, Spectra
Clinical Research is backed by more than a decade of clinical trial
expertise and nearly 30 years of central laboratory services to the
dialysis community. We support diverse clinical trials of all sizes
- making each trial and each patient our highest priority.
|
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As a division of Spectra Laboratories, we leverage the capacity
and technology of a large organization while maintaining the
flexibility and responsiveness of a small specialty laboratory. We
have participated in trials spanning therapeutic areas including
nephrology, gastroenterology, oncology, women's health, and
central nervous system (CNS) disorders. Our global support network
ensures continuous, reliable service for clinical trials in
locations worldwide including North America, Israel, India, South
America, Europe, Australia, South Africa.
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Company:
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Strata Company
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Booth:
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229
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Web:
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www.gostrata.com
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Strata Company meets the special needs of the pharmaceutical
clinical research industry by providing print and distribution of
clinical trial collateral including CRFs/data collections forms,
training/reference materials and subject recruitment
displays/collateral. To aid clinical trial professionals, Strata
offers an online campaign and document management system,
StrataTracks(R), for clinical drug trials and direct marketing
programs.
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Company:
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StatWorks, Inc.
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Booth:
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1038
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Web:
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www.StatWorks.net
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StatWorks, Inc is a full service CRO located in Research Triangle
Park, NC. We offer Biostatistics, Data Management, Medical Writing,
Project Management, EDC, Clinical Monitoring and other drug
development services. We have a 14 year history of success due to
our dedication to excellence and flexibility. We offer
cost-effective solutions without sacrificing personal service.
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Company:
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Symbio LLC
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Booth:
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401
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Web:
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www.symbioresearch.com
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Symbio is a full-service CRO with the expertise in dermatology.
Since 2002, we have a proven track record of successfully managing
Phase I-IV clinical trials. By partnering with our Sponsors, we are
involved with strategic planning throughout the entire product
development cycle.
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Company:
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TekVault
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Booth:
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2011
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Web:
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www.tekvault.com
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Software Solution for managing and sharing information with health
care professionals serving the Life Sciences/Pharmaceutical industry.
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MedAxis Software Suite:
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--Medical Information Vault
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--Physician Inquiry Vault
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--Patient Inquiry Vault
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MedAxis software disseminates information with greater efficiency,
aligned with FDA regulatory requirements.
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Also provides consulting, technology and outsourcing services.
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Company:
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The Clinical Resource Network
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Booth:
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1322
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Web:
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www.crnspg.com
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CRN is an innovative and dynamic clinical contractor and resourcing
provider. We support Sponsors and CROs with needs for experience
clinical professionals and contractor teams. Our solutions provide
significant cost savings with an emphasis on quality and service
delivery. CRNs business model differs from competitors in our niche
and provides unique value added features. If your are seeking
clinical professionals for rewarding opportunities CRN sets the
standard.
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Company:
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The Clinical Trial Company
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Booth:
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234
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Web:
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www.theclinicaltrialcompany.com
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Formed in 2002, TCTC is a privately owned full-service clinical
research provider with offices in the UK, Europe, North America and
Australia. Our philosophy is one of teamwork, positivity,
communication, responsibility and adding value. As a full service
CRO, TCTC specialises in clinical studies for pharmaceutical,
biotech and medical device companies. TCTC works with clients with
medium size clinical trials and novel products which often do not
have a classical road map to the market. The Clinical Trial Company
clinical trial process facilitates commercial efficiency and cost
effectiveness in helping bring clients' products to market.
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Company:
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The Medical Research Network
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Booth:
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123
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Web:
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http://www.themrn.co.uk/
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The Medical Research Network (MRN) is a unique clinical trial
support organisation offering nursing focused patient recruitment &
retention solutions globally for clinical trials.
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The MRN offers Site Nurse Support and Home Trial Support services
across the globe.
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Site Nurse Support - Provision of dedicated teams of research nurses
and coordinators at trial sites, aimed at identification of patients
and running of trial activities.
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Home Trial Support - Provision of nursing teams capable of
performing patient home healthcare visits in clinical trials. Such
an approach can improve recruitment rates by as much as 60% and
maintain retention above 95%.
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Contact:
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Stuart Redding, Director
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+44 (0) 7764 965 039
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[email protected]
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Company:
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Therapak Corporation
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Booth:
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1530
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Web:
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www.therapak.com
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Therapak provides 3rd party kit assembly and lab supply distribution
solutions.
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Company:
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Therapeutics Inc.
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Booth:
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839
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Web:
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www.therapeuticsinc.com
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Therapeutics, Inc. is a full service dermatology contract research
organization. The Company was founded in 1997 and has its corporate
headquarters in San Diego, CA. The dermatology expertise within our
organization is unparalleled; no similar organization employs 4
board certified Dermatologists. We have decades of experience in the
category with numerous product approvals to our credit.
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Company:
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ThreeWire, Inc.
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Booth:
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1807
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Web:
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www.threewire.com
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ThreeWire is a patient recruitment, enrollment and management
provider focused on accelerating patient recruitment and enrollment
for the medical device, pharmaceutical, and biotech industries. We
utilize a proven, flexible, systematic approach with predictable and
measurable outcome-based strategies backed by performance-based
pricing. Our high-quality customized recruitment and unique
site-based programs provide value-based solutions, including
real-time tracking and reporting, for sponsors, sites and patients
across North America and Europe.
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Company:
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TKL Research, Inc.
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Booth:
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1034
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Web:
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www.tklresearch.com
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TKL Research, Inc. is a full-service, International CRO providing
comprehensive services for conducting Phase 1-4 clinical research
studies; an inpatient Phase 1 facility and outpatient specialized
research clinics. TKL provides clients with comprehensive clinical
development services, and a competitive edge in accelerating
enrollment throughout all phases of development.
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TKL services the Pharmaceutical, Biotech, Device, Diagnostic and
OTC/Consumer Healthcare markets. Since our inception in 1944, we
have continuously delivered the highest levels of expertise and
professionalism while earning the reputation for commitment to
quality, project timelines, and tight budget control.
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At TKL Research Inc., experience and reputation for quality are
coupled with close partnering with our Sponsors to provide
customized clinical research programs.
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Company:
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Total Root Concepts, Inc.
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Booth:
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1803
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Web:
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www.totalrootconcepts.com
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Our clients say it best…"Your desire to understand the project and
the accomplishments to date, along with the obstacles ahead, truly
sets you apart from other companies."
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Total Root Concepts is a training and communications company which
provides Investigator Solutions for more effective program design,
development, and delivery. Our team of professionals works with you
to customize programs that exceed everyone's expectations.
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Our Solutions include:
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• Face-to-Face & Online Investigator Meetings,
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• Regional Update Meetings,
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• Study-Specific Websites,
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• eLearning Modules, and
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• DVD creation
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With Total Root Concepts, you deliver a different message which
drives BETTER results!
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Company:
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TrainingCampus.com
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Booth:
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540
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Web:
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www.TrainingCampus.com
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TrainingCampus.com is the first global Education Management Network.
An aggregator/consolidator of resources used by healthcare/clinical
researchers. Members of our network use our FREE Cloud-Based
Education Management Systems in order to develop-deliver-track and
document training and education activities for compliance to over
270k network users.
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Company:
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Trial By Fire Solutions
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Booth:
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650
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Web:
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http://www.simplectms.com
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Trial By Fire Solutions develops and produces SimpleCTMS, a
SaaS-based clinical trial management system with a focus on ease of
use, ease of deployment, flexibility and eClinical integration. This
smart, project management focused system bridges clinical expertise
and the best up-to-date web technology. Our client support team
combines clinical and technology experts to guide and assist your
organization and maximize the productivity gains that a streamlined
CTMS can provide.
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Company:
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TTC, llc
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Booth:
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803
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Web:
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http://ttc-llc.com/
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TTC, headquartered in Philadelphia and founded by Dr. Harold Glass,
offers the largest current database of investigator budgets from 60
countries. TTC carries five distinctive products that deliver state
of the art cost benchmarking tools. TTC combines a strong financial
base, a global reach and an experienced team of customer-focused
professionals proud to serve the industry in the management of costs
and speed of clinical trials. With nearly 100 clients who conduct
over 75% of the clinical trials around the world, TTC stands ready
to serve all companies with specific programs tailored to meet their
customized requirements.
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Company:
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University of Iowa Pharmaceuticals
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Booth:
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557
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Web:
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www.pharmacy.uiowa.edu/uip
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The University of Iowa Pharmaceuticals (UIP) is the largest and most
experienced university-affiliated FDA-registered pharmaceutical
manufacturing facility in the United States. UIP has been developing
formulations, manufacturing clinical supplies, and conducting
analytical testing in compliance with current Good Manufacturing
Practices (cGMPs) for over 36 years. Virtually every type of dosage
form can be produced. UIP serves a broad spectrum of clients
including medical research centers, pharmaceutical and biotechnology
companies, and governmental agencies. UIP is licensed by the DEA to
handle controlled substances (Schedules I - V) and capable of
handling potent/cytotoxic materials.
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Company:
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Veristat, Inc.
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Booth:
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223
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Web:
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http://www.veristat.com
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Veristat is a full-service clinical research organization (CRO) and
CDISC Registered Solution Provider with demonstrated expertise in
supporting clinical trials and regulatory submissions for
pharmaceutical, biotechnology, and medical device companies. We
offer comprehensive services, including strategic consulting,
clinical monitoring, biostatistics, SAS programming, medical
writing, and data management for a single study or an entire
clinical program, as well as preparation of integrated summary
documents and submission-ready CDISC data for your regulatory
filing. Based on over 15 years of experience, Veristat has the
expertise to provide flexible, innovative, and science-focused
services customized to our clients' needs.
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Company:
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Vitalograph
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Booth:
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1329
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Web:
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www.vitalograph.com
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Vitalograph provides innovative EDC solutions in respiratory
clinical trials:
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1. Spirotrac® Centralized Spirometry with independent expert
over-reading services
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2. NEW In2itive e-Diary for ePRO solutions - best in class
integrated spirometer/e-Diary
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3. Integrated Spirometry, Diary, Pulse Oximetry, FeNO, challenge
testing, 6MWT
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4. Bluetooth electronic PEF, FEV1 and FEV6 monitors for integration
with proprietary e-Diaries
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5. NEW unique AIM inhaler trainer for pMDIs and DPIs
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6. VIEWER web portal
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7. VitaloJAK Cough Monitor
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8. Centralized data management, project management, site and monitor
training, 24/7 support and protocol review
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Global Phase II, III, and IV studies with regular repeat business
from happy sponsors.
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Company:
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WebbWrites, LLC
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Booth:
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730
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Web:
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http://www.webbwrites.com
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WebbWrites is home to experienced professionals dedicated to
assisting pharmaceutical companies in achieving their submission
goals. Clinical writing and statistical consulting services are
provided by employees who have comprehensive knowledge of submission
requirements.
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Several important factors set WebbWrites apart from other service
providers:
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Stable company founded in 1998 that is fully committed to employees
and their families, resulting in no turnover among writing staff;
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100% full-time employees, most of whom have worked together for more
than 15 years;
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Extensive submission experience in wide variety of therapeutic
areas, having assisted Sponsor companies file more than 66 NDAs
since company inception;
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Small company, with flexibility to work in and adapt to different
Sponsor situations.
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Company:
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WebWise Learning, Inc.
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Booth:
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504
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WebWise Learning brings extensive industry knowledge together with
instructional design experience and technology expertise to develop
effective interactive online learning and job support tools for the
pharmaceutical, biotech, medical device, and healthcare industries.
We offer off-the-shelf, customizable, and custom company-specific
solutions.
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The principles of instructional design and performance consulting
are the foundation on which we build all elements of a performance
improvement system. This foundation starts with working with clients
to understand their business goals and analyzing the business
environment.
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Company:
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West Coast Clinical Trials
|
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Booth:
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804
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Web:
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www.wcct.com
|
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West Coast Clinical Trials (WCCT) is a full service early
development CRO with 2 locations in Orange County, California. We
provide regulatory support for IND filing, drug development
planning, clinical study execution, project management, back-end
data management and report services. We focus on healthy volunteer
trials as well as special populations.
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Company:
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Whitsell Innovations, Inc
|
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Booth:
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2039
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Web:
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http://www.whitsellinnovations.com/
|
|
Whitsell Innovations (WI), Inc. is a full-service medical and
scientific writing company. WI employees write regulatory documents
from the preclinical stage (including chemistry, manufacturing, and
controls documentation) through all clinical stages (IND
submissions, protocols, Investigator Brochures, Clinical Study
Reports, narratives, NDA submissions, etc.) Our expertise includes
manuscript, slide, and abstract preparation for scientific,
pharmaceutical, biotech, and device clients. We craft sales aids and
modules and perform literature reviews. We write and edit continuing
medical education content and book chapters for accredited
institutions and firms. Our singular focus is perfect scientific and
medical communication directed at our client's target audience.
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