More information: Alexander O Everhart et al, Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study, BMJ (2025). DOI: 10.1136 ...

DUBLIN--(BUSINESS WIRE)--The "Latest Chinese Guidebook for Medical Device Adverse Events Reporting, Monitoring and Re-Evaluation" report has been added to ResearchAndMarkets.com's offering.

Dublin, March 18, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" has been added to ResearchAndMarkets.com's offering.

A significant number of medical device adverse events that resulted in patient deaths were miscategorized in the FDA's Manufacturer and User Facility Device Experience (MAUDE) database ...

Dublin, Nov. 03, 2022 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" conference has been added to ResearchAndMarkets.com's ...

The Materiovigilance Programme of India (MvPI), under the Indian Pharmacopoeia Commission, has released the updated version of the medical devices adverse event reporting form, for the use of ...

Early adverse events after left ventricular device implantation significantly ... of the Heart Failure and Heart Transplant Program at Medical University of South Carolina, told Healio.

Dublin, March 18, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" has been added to ResearchAndMarkets.com's offering. This ...