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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...
November 08, 2024 04:52 ET | Source: Research and Markets

Mastering DHF, DMR, and DHR Course: Essential Documentation in Medical Device Manufacturing (ONLINE EVENT: November 26, 2024/ON-DEMAND)

Dublin, Nov. 08, 2024 (GLOBE NEWSWIRE) -- The "Mastering DHF, DMR, and DHR: Essential Documentation in Medical Device Manufacturing Webcast" webinar has been added to ResearchAndMarkets.com's...
June 27, 2024 10:06 ET | Source: Research and Markets

FDA e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo Course (ON-DEMAND)

Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo" training has been added to ResearchAndMarkets.com's offering.The regulation and...
June 11, 2024 07:03 ET | Source: Research and Markets

Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations: Four Day Online Event - November 18-21, 2024

Dublin, June 11, 2024 (GLOBE NEWSWIRE) -- The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" course has been added to ResearchAndMarkets.com's offering. This...
April 08, 2024 10:39 ET | Source: Research and Markets

Intensive 1 Day Pharmaceutical and Medical Device Human Factors and Usability Engineering Process Course (ONLINE EVENT)

Dublin, April 08, 2024 (GLOBE NEWSWIRE) -- The "An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals" conference has been added to ResearchAndMarkets.com's offering....
March 29, 2024 05:08 ET | Source: Research and Markets

4 Day Virtual Medical Device Software Compliance Course: Complying with the EU MDR, EU IVDR & FDA Regulations

Dublin, March 29, 2024 (GLOBE NEWSWIRE) -- The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. ...
January 17, 2024 13:53 ET | Source: Research and Markets

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...
January 17, 2024 10:43 ET | Source: Research and Markets

An Online FDA and EU Technical Documentation Training Course: Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - Earn up to 4.0 RAC Credits

Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - A Technical Documentation Training" training has been added to...

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