Good Deviation Practice - CAPA Process - 2017

Overview:
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.

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

Who will benefit:
Compliance Manager
Process Engineer
Production Manager
Regulatory Manager
Quality Manager

Speaker Profile:
John R. Godshalk currently works for the Biologics Consulting Group as a Senior Consultant. John served as a Senior Review Biochemical Engineer and Lead cGMP inspector in the Division of Manufacturing and Product Quality at CBER, FDA. He contributed to formulation of FDA policy.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

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WHEN AND WHERE

03 May 2017
United States of America

ORGANIZER

Compliance4All

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Added 7 years ago by Compliance4All on Education , Health and Medicine , Health , Medical ethics , Public Health