Good Deviation Practice: what you need to know - Webinar By GlobalCompliancePanel

This course explores the deviation and CAPA processes and best practices for both. It shows how to avoid pitfalls and minimize regulatory scrutiny by having a robust deviation/CAPA system and thorough investigations. 

The deviation process is explored and evaluated and examples are given to demonstrate the best way to handle deviations and subsequent CAPAs. Attendees will have the opportunity to interact and ask questions about best practices regarding both devotions and the CAPA process.  Reasons for having a robust deviation process are given with examples.

Why you should attend: The attendee will learn the best practices for the deviation process and the important points from a regulatory standpoint.

Areas Covered In the Session:

Explores typical deviation and CAPA processes within the Quality System Explores best practices for the deviation and CAPA processes Explores best practices for documentation  Tips on how to avoid possible pitfalls with deviations Tips on minimizing regulatory scrutiny with deviations Examples of good deviation write-ups, investigations and CAPAs

Who will benefit:

Compliance Manager Process Engineer Production Manager Regulatory Manager Quality Manager

Thursday, August 4, 2011  
10:00 AM PDT | 01:00 PM EDT

 

Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00   webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com   Phone: 800-447-9407 Fax: 302-288-6884