How To Avoid FDA 483’s/ Warning Letters? What to Do If You Happen to Get One? 2015
30 Jul 2015
Webinar
Description
Topics
Causes of Form 483 / Warning Letter
FDA Inspections - background
Best Practices for Responding to 483
Some recent results of companies failing to respond appropriately
What to do if the responses fail
Best Practices for Responding to Warning Letter
Who should Attend
Regulatory Affairs professionals
CEOs
IT
Quality
Small business owners
Engineers
Consultants
GxP
Past Events
How To Avoid FDA 483’s/ Warning Letters? What to Do If You Happen to Get One? 2015 - 30 Jul 2015, Webinar (53146)
Important
Please, check "How To Avoid FDA 483’s/ Warning Letters? What to Do If You Happen to Get One?" official website for possible changes, before making any traveling arrangements
