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
November 15, 2023 08:58 ET
|
Research and Markets
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...
Navigating Complex Regulatory Terrain: Understanding MDR Classification, Risk Management, and Compliance for Software (December 11-14, 2023)
November 03, 2023 09:08 ET
|
Research and Markets
Dublin, Nov. 03, 2023 (GLOBE NEWSWIRE) -- The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. ...
MedReg 2023: Annual Medical Device Regulatory Confex - Unveil the Future of Regulatory Compliance
August 16, 2023 07:48 ET
|
Research and Markets
Dublin, Aug. 16, 2023 (GLOBE NEWSWIRE) -- The "MedReg 2023 - Annual Medical Device Regulatory Confex" training has been added to ResearchAndMarkets.com's offering. Step into the realm of...
Gain an Understanding of ISO 14971: Risk Management in the Medical Device Industry Webinar
April 12, 2023 11:28 ET
|
Research and Markets
Dublin, April 12, 2023 (GLOBE NEWSWIRE) -- The "Risk Management in the Medical Device Industry - Understand Iso 14971" training has been added to ResearchAndMarkets.com's offering. Medical...
2 Day Online Course Covering Risk Management in the Medical Devices Market
March 03, 2021 07:13 ET
|
Research and Markets
Dublin, March 03, 2021 (GLOBE NEWSWIRE) -- The "Risk Management in Medical Devices Industry" conference has been added to ResearchAndMarkets.com's offering. Risk management is a mandatory and...