Wednesday, August 21, 2013

Process Validation for Medical Devices

August 21, 2013 at 8am to August 22, 2013 at 5pm – Courtyard Marriott Boston ,MA 02139, USA Medical device manufacturers can avoid FDA Warning Letters, 483s and enforcement actions with a good understanding process validation principles. But knowing how to proceed is the toughest task as no… Organized by ComplianceOnline | Type: seminar