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How to design a CAPA system that meets and exceeds compliance requirements

This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements

 
PRLog - Aug. 11, 2011 - HOUSTON -- 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.


Price List: Live : $189.00 Corporate live : $499.00 Recorded : $249.00, CD:$299.00

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

https://www.compliance2go.com/index.php?option=com_traini...

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Contact Email:
***@compliance2go.com Email Verified
Source:subscribe@compliance2go.com
Phone:877.782.4696
Zip:77042
City/Town:Houston - Texas - United States
Industry:Biotech
Tags:compliance training, conference, e-learning, Education, event, fda, web seminar, webinar, compliance2go, medical device
Shortcut:prlog.org/11621406
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