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November 26, 2025 04:09 ET | Source: Research and Markets

1 Day Virtual Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training Course

Dublin, Nov. 26, 2025 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (Nov 13, 2025)" training has been...
November 26, 2025 04:03 ET | Source: Research and Markets

1 Day Online Course: EU Regulations for Digital Medical Devices with AI Components: What Does a Manufacturer Need to Consider? (Dec 9, 2025)

Dublin, Nov. 26, 2025 (GLOBE NEWSWIRE) -- The "The EU Regulations for Digital Medical Devices with AI Components - A Basket Full of Requirements - What Does a Manufacturer Need to Consider? (Dec 9,...
November 05, 2025 10:57 ET | Source: Research and Markets

Mobile Medical Device Apps and the FDA Training Webinar: Classification, Regulatory Requirements and Cybersecurity

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Mobile Medical Device Apps and the FDA - Classification, Regulatory Requirements and Cybersecurity" training has been added to ...
November 05, 2025 10:06 ET | Source: Research and Markets

FDA 510(k) Modernization, Breakthrough Device, and Safer Technologies Programs (STeP) Training Webinar

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "510(k) Modernization, Breakthrough Device, and Safer Technologies Programs (STeP) (Oct 8, 2025)" training has been added to ResearchAndMarkets.com's...
September 29, 2025 05:00 ET | Source: Research and Markets

An introduction to Risk Management ISO 14971:2019 Training Course: Learn to Review and Build Documentation to Meet Quality and Regulatory Standards (Nov 11, 2025)

Dublin, Sept. 29, 2025 (GLOBE NEWSWIRE) -- The "An introduction to Risk Management ISO 14971:2019 Training Course (Nov 11, 2025)" training has been added to ResearchAndMarkets.com's offering. ...
August 06, 2025 04:21 ET | Source: Research and Markets

EU Regulations for Digital Medical Devices with AI Components Specialist Course | A Basket Full of Requirements - What Does a Manufacturer Need to Consider? (ONLINE EVENT: October 7, 2025)

Dublin, Aug. 06, 2025 (GLOBE NEWSWIRE) -- The "The EU Regulations for Digital Medical Devices with AI Components - A Basket Full of Requirements - What Does a Manufacturer Need to Consider?"...
July 18, 2025 08:42 ET | Source: Research and Markets

Two-Day FDA & MDR Training: Strengthen Post-Market Surveillance, Risk, and CAPA Systems (Online Training Course: August 25-26, 2025)

Dublin, July 18, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems (Online Training Course: August 25-26, 2025)" has been...
April 03, 2025 10:54 ET | Source: Research and Markets

Medical Devices Post Market Surveillance and Complaint Handling Systems Course: U.S. FDA CGMP Expectations/Requirements (ONLINE EVENT: May 22-23, 2025)

Dublin, April 03, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ...
January 21, 2025 09:24 ET | Source: Research and Markets

Virtual Course: Developing Effective Medical Devices Post Market Surveillance and Complaint Handling Systems Under Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act)

Dublin, Jan. 21, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ResearchAndMarkets.com's...
December 04, 2024 05:04 ET | Source: Research and Markets

U.S. FDA CGMP Expectations/Requirements for Post Market Surveillance and Complaint Handling Training Webinar (ONLINE EVENT: December 11-12, 2024)

Dublin, Dec. 04, 2024 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ResearchAndMarkets.com's...