Online Webinar :FDA GMP compliance: Investigations and deviations

Website http://c2gowebinars.com/product/?topic=investigations-deviations | Edit Freely

Category

Deadline: July 19, 2016 | Date: July 19, 2016

Venue/Country: Online, U.S.A

Updated: 2016-06-09 16:44:49 (GMT+9)

Call For Papers - CFP

Creating and Maintaining a GMP Quality System

Why should you attend :

This webinar will explain the basic principles of Deviations and Investigations in the pharmaceutical and medical device industries. Particular emphasis will be the specific requirements set out in 21 CFR Part 210/211/820 and how these requirements can be met.

Areas Covered in the Session:

SOP and documentation requirements, conducting deviations and investigations, deviation tracking

Who will benefit: (Titles)

Quality control professionals

Quality assurance professionals

Operations and management in a FDA regulated environment

Webinar includes:

Q/A Session with the Expert to ask your question

PDF print only copy of PowerPoint slides

60 Minutes Live Presentation

Certificate of attendance

For Registration :http://c2gowebinars.com/product/?topic=investigations-deviations

Note: Use coupon code    and get 15% off on registration.