Live Webinar-how To Design A Capa System That Meets Compliance Requirements

July 14, 2011 - PRLog -- Summary
This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements.

Details
Discount : Get 15 % Discount as a early bird registrations. Use Promocode CGO15

Why should you attend - CAPA is the most audited Quality subsystem by the FDA.57% of all warning letters send to organizations by the FDA in 2010 were CAPA RELATED.The trend seems to be continuing this year.

Areas Covered in the Session (Bullet points about the proceedings )

CAPA defined
The capa life cycle
CAPA requirements
CAPA design
CAPA documentation
Who will benefit: (Titles)

Quality managers
Quality Engineers
Process Engineers
Manufacturing Engineers
About the speaker:

Mr. Muchemu has over fifteen years experience in Medical Device, Pharmaceutical, Biomedical and Tissue industries as CAPA Training Instructor, Process validation Instructor, Change control Instructor, and CGMP consultant. He has held major positions at Abbott labs, Genentech, Boston Scientific, and Johnson and Johnson. He holds degrees in Biology, Chemical Engineering, and is currently working an MBA with a concentration in Public Health. He is an established author of several GMP books.

For any assistance contact us at suppor@compliance2go.com or call us at 877.782.4696