Clinical research sites for biopharma and medical device companies are seeing a substantial increase in FDA audits, which is why it is important for site personnel to consistently review processes, training, and regulations in preparation for an FDA audit. We are pleased to announce that Pearl Pathway’s own Gretchen Bowker will be presenting a webinar on this topic in December for the Society of Clinical Research Sites. Topics will include a review of FDA/OHRP regulations, best practices and tips for success, what to do and say, and how to prepare clinical sites for FDA audits.
Title: Preparing for an FDA audit
When: December 16, 2014 @ 12:00pm ET
Price (non-SCRS members): $79.00
Members are free!
Sponsored By: Acurian
For more information and registration, click here.