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Webinar On Master Validation Planning To Meet US FDA cGMP ISO 13485 and ICH Q9 ISO 14971 Req

3/5/2014 12:00 PM - 1:00 PM

This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies, many going back to insufficient, poor or non-existent V&V planning.

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