Risk-Based Verification and Validation Planning to Meet US FDA and ISO 13485 Requirements
Website https://www.complianceonline.com/risk-based-verification-and-validation-planning-to-meet-us-fda-and- |
Edit Freely
Category
Deadline: June 05, 2019 | Date: June 05, 2019
Venue/Country: U.S.A
Updated: 2019-05-23 22:24:08 (GMT+9)
Call For Papers - CFP
FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based V&V planning. This webinar will teach you how to develop a master validation plan by evaluating its elements against ISO 14971 hazard analysis / risk management for development of meaningful product validations.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.