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SynteractHCR Experts Continue Presentations at U.S. and European Events Focused on Outsourcing in Clinical TrialsFull-service, international, contract research organization (CRO) SynteractHCR will offer speaker presentations and exhibits at the Outsourcing in Clinical Trials Europe event in Paris, May 17-18, and at the Outsourcing in Clinical Trials East Coast conference, May 25-26, in King of Prussia, Pennsylvania. Both conferences feature thought leaders who address pressing regulatory topics and electronic innovation that will increase the knowledge base of drug development sponsors worldwide. At OCT Europe, the company will exhibit in booth #61. Director of Regulatory Affairs, Europe, Ludwig Baumann, will present, "The New EU Clinical Trials Regulation: What Does it Change and What Will the Impact Be to Drug Development in the EU?" on Wednesday, May 18th at 9:15 a.m. His presentation will address the rationale behind changing the previous clinical trials directive as well as the following:
At OT East Coast, SynteractHCR will exhibit at booth #68 and will present its expertise in electronic submission handling. On Wednesday, May 25th at 4:30 p.m., Senior Regulatory Affairs Manager Thomas Christensen will present, "Preparing Proactively for FDA Mandated eCTD Submissions." Because the FDA will require electronic common technical document (eCTD) submissions starting in 2017, attendees will learn how to streamline eCTD preparation as it becomes the standard submission format. The presentation will cover:
Attendees interested in meeting with the SynteractHCR team at these events may contact Executive Director of Business Development Kim Martinez at 760-529-3440 or [email protected]. See SynteractHCR's full schedule of events and follow its social channels on LinkedIn and Twitter for live updates during all conferences.
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