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18. Juli 2025 08:42 ET | Quelle: Research and Markets

Two-Day FDA & MDR Training: Strengthen Post-Market Surveillance, Risk, and CAPA Systems (Online Training Course: August 25-26, 2025)

Dublin, July 18, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems (Online Training Course: August 25-26, 2025)" has been...
03. April 2025 10:54 ET | Quelle: Research and Markets

Medical Devices Post Market Surveillance and Complaint Handling Systems Course: U.S. FDA CGMP Expectations/Requirements (ONLINE EVENT: May 22-23, 2025)

Dublin, April 03, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ...
21. Januar 2025 09:24 ET | Quelle: Research and Markets

Virtual Course: Developing Effective Medical Devices Post Market Surveillance and Complaint Handling Systems Under Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act)

Dublin, Jan. 21, 2025 (GLOBE NEWSWIRE) -- The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ResearchAndMarkets.com's...
04. Dezember 2024 05:04 ET | Quelle: Research and Markets

U.S. FDA CGMP Expectations/Requirements for Post Market Surveillance and Complaint Handling Training Webinar (ONLINE EVENT: December 11-12, 2024)

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...
17. Januar 2024 13:53 ET | Quelle: Research and Markets

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

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...
15. November 2023 08:58 ET | Quelle: Research and Markets

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

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...
30. Dezember 2022 04:53 ET | Quelle: Research and Markets

2 Day Medical Device Post-Market Regulations and Challenges Online Course: Complaint Handling, MDR Reporting and Recalls Course (January 26-27, 2023)

Dublin, Dec. 30, 2022 (GLOBE NEWSWIRE) -- The "A Comprehensive View of Medical Device Post-Market Regulations and Challenges -Complaint Handling, MDR Reporting and Recalls Course" training has been...
01. Juli 2022 04:43 ET | Quelle: Research and Markets

Medical Devices Post Market Surveillance Online Course: Product Complaints Management, Medical Device Reporting, Vigilance Reporting, Product Recalls (July 29, 2022)

Dublin, July 01, 2022 (GLOBE NEWSWIRE) -- The "Medical Devices - Post Market Surveillance: Product Complaints Management, Medical Device Reporting, Vigilance Reporting, Product Recalls" training has...