1. Live Webinar on : How to design a CAPA System that meets Compliance Requirements - Thursday 08 September 2011 (60 Minute) Get 15 % Discount as a early bird registrations. Use Promo Key : CGO15 Who will benefit Quality managersQuality EngineersProcess EngineersManufacturing Engineers PricingLive ( Single registration ) : $189.00Group ( Max 10 Attendee): $499.00More Trainings Description This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements.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 yearAreas Covered in the Seminar:CAPA definedThe CAPA life cycleCAPA requirementsCAPA designCAPA documentation.About 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 877.782.4696https://www.compliance2go.com/index.php?option=com_training&speakerkey=4&productKey=18Compliance2go | www.Compliance2go.com Phone : 877.782.4696 | Fax : 281-971-0286 Email : Support@compliance2go.com<br />