Good Deviation Practice - CAPA Process - 2017

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Category Good Deviation Practice, Standard Deviation, CAPA process, std meaning, standard deviation calculator, standard deviation formula, deviation, calculating standard deviation, standard deviation example

Deadline: May 02, 2017 | Date: May 03, 2017

Venue/Country: Online, U.S.A

Updated: 2017-03-21 16:17:43 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com