Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions

This webinar will help attendees understand the fundamental steps of a deviation investigation with focus on using facts and objective evidence to arrive at root cause and CAPA. Learn how to identify and avoid potential pitfalls during deviation investigations.

Why Should You Attend:

One of the most common FDA 483 and Warning Letter citations continues to be inadequate investigations. The FDA continues to find fault with investigations and the stated conclusions. The FDA clearly expects that deviation investigations determine what happened, why it happened, and what was done to prevent it from happening again.

Who Will Benefit:

Deviation investigators

Reviewers and approvers of deviation investigations (e.g. Dept. Heads, Quality Assurance)

QA staff and management

Regulatory Affairs staff and management

QC staff and management

Instructor Profile:

Andrew Campbell, has 25 years of pharmaceutical quality assurance and quality systems experience in both industry and consulting roles. Mr. Campbell has worked in clinical supply and commercial manufacturing environments, and has experience with integrated manufacturing and contract manufacturing business models.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/deviation-investigation-best-practices-ensuring-correct-content-and-conclusions-webinar-training-703538-prdw?channel=sciencedz