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Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations: Four Day Online Event - November 18-21, 2024
June 11, 2024 07:03 ET | Research and Markets
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...
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Intensive 1 Day Pharmaceutical and Medical Device Human Factors and Usability Engineering Process Course (ONLINE EVENT)
April 08, 2024 10:39 ET | Research and Markets
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....
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4 Day Virtual Medical Device Software Compliance Course: Complying with the EU MDR, EU IVDR & FDA Regulations
March 29, 2024 05:08 ET | Research and Markets
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. ...
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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
January 17, 2024 13:53 ET | Research and Markets
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...
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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
January 17, 2024 10:43 ET | Research and Markets
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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Intensive 1 Day Virtual Course on Introduction to Human Factors for Pharmaceutical and Medical Device Professionals: Ethics, Consent and User Safety Along with How ISO 14971:2019 is Used
December 22, 2023 04:38 ET | Research and Markets
Dublin, Dec. 22, 2023 (GLOBE NEWSWIRE) -- The "An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals" conference has been added to ResearchAndMarkets.com's offering. ...
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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...
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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. ...
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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...
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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...