Parexel Expands Network of Global Regulatory Experts
BOSTON and DURHAM, N.C., Sept. 08, 2022 (GLOBE NEWSWIRE) -- Parexel, a leading global clinical research organization (CRO) focused on development and delivery of innovative new therapies to advance patient health, today announced the appointment of five former regulators to its Regulatory & Access Consulting team, further accelerating the advancement of new treatments for patients worldwide.
“Parexel has proven to be a reliable and effective regulatory partner in helping our enterprise and biotech customers address ever-evolving regulatory changes and compete on a global scale,” said Paul Bridges, Executive Vice President, Regulatory & Access, Parexel. “These new colleagues bring the critical first-hand and global experience our customers need to seamlessly navigate the regulatory landscape, de-risk their portfolios and ultimately deliver innovative new therapies to patients around the world.”
The new leaders join Parexel’s more than 1,000 seasoned experts whose combined knowledge, skill and experience in quality and compliance expertly guide customers through complex global and in-country regulations. They will provide their insight and expertise on key aspects of the regulatory process, including navigating rapidly evolving landscapes related to regulatory meetings and submissions, compliance and market access.
“Innovation in drug development creates new pathways to bring more targeted medicines to market and improve the design and efficiency of clinical trials,” said Jamie Macdonald, Chief Executive Officer, Parexel. “Our new regulatory experts bring significant tenure with global health authorities along with a breadth of therapeutic expertise — from rare disease to oncology and hematology and including complex modalities such as cell and gene therapy and monoclonal antibodies — to leverage this innovation and navigate global regulatory processes to bring new therapies to patients faster.”
The recent appointments include:
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