Medical Products Reporting Program

MedWatch: FDA Safety Information & Adverse Event …

https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program

MedWatch, the FDA’s medical product safety reporting program for health professionals, patients and consumers. Report a Problem Safety Information Stay Informed MedWatch receives reports...

MedWatch Forms for FDA Safety Reporting | FDA

https://www.fda.gov/safety/medical-product-safety-information/medwatch-forms-fda-safety-reporting

Medical Device Reporting (MDR): How to Report Medical …

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems

Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and …

Reporting Adverse Events to FDAs MedWatch Program

https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program/information-about-reporting-adverse-events-fdas-medwatch-program

An important FDA program called "MedWatch" allows health care professionals and consumers to report serious problems that they believe may be associated with the …