FDA e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo Course (ON-DEMAND)
June 27, 2024 10:06 ET
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Research and Markets
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...
An Introduction to the Design and Development of Medical Devices: 2-Day Online Training Course (July 24-25, 2024) with CPD Certification - A Comprehensive Appraisal of Key Aspects
May 30, 2024 04:20 ET
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Research and Markets
Dublin, May 30, 2024 (GLOBE NEWSWIRE) -- The "An Introduction to the Design and Development of Medical Devices Training Course" conference has been added to ResearchAndMarkets.com's offering. ...
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
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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...
3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS
December 15, 2023 06:13 ET
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Research and Markets
Dublin, Dec. 15, 2023 (GLOBE NEWSWIRE) -- The "3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS" webinar has been added to ...