FDA Submission: The New Rules

Save the date and register now for our next session of the Silicon Valley BioTalks:

FDA Submission: The New Rules
June 6th, 2012 | 6.00 PM | South San Francisco

Clinical and regulatory experts will share their experience on June 6th to help you understand the evolving regulatory requirements and to better prepare for a successful FDA submission.

This event is FREE with pre-registration before May 26th, 2012. Click here for event details.

Discussion topics include:

• How can clinical trial professionals overcome the increased complexity and cost of clinical trials?
• Which best practices help adapt to the new trends and FDA requirements?
• What are the do's and don'ts for a successful FDA submission?

A unique venue to share industry best practices and to network

A panel composed of clinical and regulatory experts with extensive industry experience:

• Christine Conroy, VP, Regulatory Affairs and GCP Compliance at Affymax
• Sandra Nino-Siddens, Executive Director, Regulatory Affairs at Geron
• Moderated by Dr. Anne-Marie Duliege, Chief Medical Officer at Affymax

An exciting networking session: The event starts with a networking session with food and drinks. Join us and take the opportunity to meet clinical trials professionals and local industry experts. 

"A truly informative panel discussion"

"A great forum to hear some very experienced clinical trial professionals"

"It attracted participants from all over the Bay Area, and beyond"  

AN EVENT SPONSORED BY

Clinovo

Capgemini Consulting

French American Chamber of Commerce in San Francisco