Variance from Manufacturer Report Number Format [MDR letter]
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Adverse Event Reporting
Published
July 15, 1996
Last updated
April 27, 2021
Description
This document is a guidance document titled "Variance from Manufacturer Report Number Format [MDR letter]" and it discusses adverse event reporting.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)