Good Deviation Practice - CAPA Process - 2017

What topics are covered by the course?

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 should attend?

Compliance Manager
Process Engineer
Production Manager
Regulatory Manager
Quality Manager

What will I be able to do on completion?

Reasons for having a robust deviation process are given with examples.

How will I be assessed?

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501114LIVE?channel=coursesplus_Jun_2017_SEO

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: support@compliance4All.com

Guide Price: $ 150

Delivery: Online
Category: Health & Medical »
Duration: 10:00 AM to 11:00 AM
Qualification: N/A

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