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Join the A-Team in California for the largest and most recognized meeting of global regulatory affairs professionals

Connect with Allucent’s regulatory and drug development consulting experts at booth #1021 to learn more about how to successfully navigate the ever-changing regulations that are essential to the clinical trial process.
 

Session - Optimizing Health Authority interaction outcomes using an integrated strategy and multidisciplinary global regulatory and product development team

11:15am – 11:50am – Wednesday, September 18
Exhibit Hall: Ignite Theater (939)

Join our panelists as they explore the advantages of a global, interdisciplinary approach in planning, preparing for and attending regulatory agency meetings, available global submission initiatives and projects, and less formal interactions with Health Authorities. Panelists will share experiences and lessons learned and invite discussion on optimizing a global product development regulatory pathway.

Panelists: 
Nadine Bouchard - Vice President Regulatory Affairs, Head of Project Management, Allucent
Sheila R. Plant​ - Senior Director, Regulatory Affairs, Allucent
Joshua Taylor - Senir Director, Regulatory Affairs – Head of Clinical Strategy, Allucent

 

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