Join the A-Team in Pittsburgh for RAPS Convergence, the largest gathering of global regulatory affairs professionals.
Connect with Allucent’s regulatory and drug development consulting experts at booth #837 during RAPS Convergence USA, to learn how we guide our clients to successfully navigate the ever-changing regulations that are essential to the clinical trial process.
SESSION DETAILS:
Title: Proactivity and Best Practices in the Evolving FDA Landscape
Date/Time: Wednesday 8th October, 10.45 – 11.10
Location: Exhibit Hall: Ignite Theater
Speakers:
Sheila R. Plant, PhD, MHS, RAC – Sr. Director, Regulatory Affairs
Joshua Taylor, PhD, RAC – Sr. Director, Regulatory Affairs, Head of Clinical Strategy
Matthew Hight – Associate Director, Regulatory Affairs
Bianca Quade, PhD – Regulatory Affairs Scientist I
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