How To Avoid 483’s/ Warning Letters | Webinar

Audits by the FDA are perhaps the most intimidating of all events at a regulated facility. Each year, the FDA conducts several thousand audits, approximately half of which lead to findings that result in Form 483s. Most Form 483 audits are amicably resolved, but a few lead to serious consequences for the audited parties, starting with Warning Letters and ending with heavy fines and jail time for a few.

This webinar on responding to FDA 483s and Warning Letters will provide tips for avoiding FDA 483s and warning letters, and train you on the best practices in responding to a 483 or warning letter so that you can manage the consequences of the findings from escalating.

Angela Bazigos will be the speaker, she is the CEO of Touchstone Technologies Inc. She has 30 years of experience in the Lifesciences industry spanning Project Management, Quality Assurance and Regulatory Affairs.

Live - Single Attendee $199.00
Live - Group $799.00
Event Duration: 2 Hours
Event Start Time: 10 AM PST | 1 PM EST

For more details call Complystream at: (+1) 844 498 6361