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11 févr. 2026 05h53 HE | Source: Research and Markets

Global Medical Devices Regulatory Affairs Handbook 2026: Country-Specific Regulatory Systems, ISO Standards, Clinical Trial Requirements, and Comprehensive Application Documentation Guidance

Dublin, Feb. 11, 2026 (GLOBE NEWSWIRE) -- The "Global Handbook of Medical Devices Regulatory Affairs" directory has been added to ResearchAndMarkets.com's offering.This Handbook is the definitive...
11 févr. 2026 05h45 HE | Source: Research and Markets

European Medical Devices Regulatory Affairs Handbook 2026: Country-Specific Regulatory Systems, ISO Standards, Clinical Trial Requirements, and Application Documentation Frameworks

Dublin, Feb. 11, 2026 (GLOBE NEWSWIRE) -- The "European Handbook of Medical Devices Regulatory Affairs" directory has been added to ResearchAndMarkets.com's offering.This Handbook is the definitive...
30 janv. 2026 04h06 HE | Source: Research and Markets

EU (European Union) and UK Medical Device Regulation (MDR) and the In-Vitro Diagnostic Regulation (IVDR) Update Training Course (Online Event: April 29, 2026)

Dublin, Jan. 30, 2026 (GLOBE NEWSWIRE) -- The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Apr 29, 2026)"...
30 janv. 2026 04h01 HE | Source: Research and Markets

Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions Webinar

Dublin, Jan. 30, 2026 (GLOBE NEWSWIRE) -- The "Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions (January 15, 2026)" training has been added to ...
29 janv. 2026 04h07 HE | Source: Research and Markets

Sterilization of Medical Devices Training Course: ISO Frameworks, Microbiology Methods, and Radiation, Ethylene Oxide, and Moist Heat Validation (Online Event: Apr 23rd - Apr 24th, 2026)

Dublin, Jan. 29, 2026 (GLOBE NEWSWIRE) -- The "Sterilization of Medical Devices Training Course (Apr 23rd - Apr 24th, 2026)" training has been added to ResearchAndMarkets.com's offering. Sterile...
28 janv. 2026 04h01 HE | Source: Research and Markets

UK Medical Devices Conformity Assessed (UKCA) Marking Training Course: Marking Requirements, Transitional Rules, and Strategic Alignment to Ensure Regulatory Compliance (Online Event: Apr 15, 2026)

Dublin, Jan. 28, 2026 (GLOBE NEWSWIRE) -- The "UK Conformity Assessed (UKCA) Marking for Medical Devices Training Course (Apr 15, 2026)" training has been added to ResearchAndMarkets.com's...
15 janv. 2026 11h54 HE | Source: Research and Markets

An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices: Online Training Course (May 14th, 2026)

Dublin, Jan. 15, 2026 (GLOBE NEWSWIRE) -- The "An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Training Course (May 14, 2026)" training has been added to ...
14 janv. 2026 11h45 HE | Source: Research and Markets

Medical Device Regulations in the Middle East and North Africa (Online Training Course: May 18th-19th, 2026) - A Focus on Regulatory Requirements and Developments in Individual Countries

Dublin, Jan. 14, 2026 (GLOBE NEWSWIRE) -- The "Medical Device Regulations in the Middle East and North Africa Training Course (May 18th - May 19th, 2026)" has been added to ResearchAndMarkets.com's...
23 déc. 2025 07h59 HE | Source: Research and Markets

Medical Device Regulations in Asia-Pacific Markets Training Course: Knowledge and Practical Guidance Needed to Navigate Compliance and Successfully Access These High-growth Markets (Mar 3-4, 2026)

Dublin, Dec. 23, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Regulations in Asia-Pacific Markets Training Course (Mar 3rd - Mar 4th, 2026)" training has been added to ResearchAndMarkets.com's...
23 déc. 2025 07h51 HE | Source: Research and Markets

The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course (Online Event: Mar 4, 2026)

Dublin, Dec. 23, 2025 (GLOBE NEWSWIRE) -- The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation)...

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