RSS Events Feeds

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.

Events Map

Email Newsletters

Want to be up-to-date with the latest news and updates from To subscribe, just give us your email address below; you'll choose which e-newsletters you'd like to receive on the next screen.