U.S. FDA CGMP Expectations/Requirements for Post Market Surveillance and Complaint Handling Training Webinar (ONLINE EVENT: December 11-12, 2024)
04 déc. 2024 05h04 HE
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Research and Markets
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...
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...
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...
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations: Four Day Online Event - November 18-21, 2024
11 juin 2024 07h03 HE
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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...
Intensive 1 Day Pharmaceutical and Medical Device Human Factors and Usability Engineering Process Course (ONLINE EVENT)
08 avr. 2024 10h39 HE
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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....
4 Day Virtual Medical Device Software Compliance Course: Complying with the EU MDR, EU IVDR & FDA Regulations
29 mars 2024 05h08 HE
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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. ...
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
17 janv. 2024 13h53 HE
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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...
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...
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
22 déc. 2023 04h38 HE
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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. ...
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
15 nov. 2023 08h58 HE
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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...