Webinar Examining Section 522 of the Federal Food, Drug, and Cosmetic Act: FDA CGMP Medical Device Expectations/Requirements for Post Market Surveillance and Complaint Handling Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ResearchAndMarkets.com's...

2 Day Virtual Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) Seminar: U.S. FDA CGMP Expectations/Requirements for Post Market Surveillance and Complaint Handling Dublin, Nov. 15, 2023 (GLOBE NEWSWIRE) -- The "Establish a Compliant Medical Device Post Market Surveillance and Complaint Handling System" training has been added to ResearchAndMarkets.com's...

2 Day Medical Device Post-Market Regulations and Challenges Online Course: Complaint Handling, MDR Reporting and Recalls Course (January 26-27, 2023) Dublin, Dec. 30, 2022 (GLOBE NEWSWIRE) -- The "A Comprehensive View of Medical Device Post-Market Regulations and Challenges -Complaint Handling, MDR Reporting and Recalls Course" training has been...

Medical Devices Post Market Surveillance Online Course: Product Complaints Management, Medical Device Reporting, Vigilance Reporting, Product Recalls (July 29, 2022) Dublin, July 01, 2022 (GLOBE NEWSWIRE) -- The "Medical Devices - Post Market Surveillance: Product Complaints Management, Medical Device Reporting, Vigilance Reporting, Product Recalls" training has...