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

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com

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.