Mastering DHF, DMR, and DHR Course: Essential Documentation in Medical Device Manufacturing (ONLINE EVENT: November 26, 2024/ON-DEMAND)
08 nov. 2024 04h52 HE
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Research and Markets
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...
Final Days to Register: Intensive 2 Day Introduction to the Design and Development of Medical Devices Training Course (ONLINE EVENT/ON-DEMAND)
15 oct. 2024 10h33 HE
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Research and Markets
Dublin, Oct. 15, 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. ...
FDA e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo Course (ON-DEMAND)
27 juin 2024 10h06 HE
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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
30 mai 2024 04h20 HE
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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
17 janv. 2024 10h43 HE
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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
15 déc. 2023 06h13 HE
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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 ...