IMDRF Consults on Use of Registries to Support Device Approval Decisions
By Zachary Brennan -
Published 02 October 2017
The International Medical Device Regulators Forum (IMDRF) has opened for consultation until 1 December a third document on examining the use of registries to support medical device regulatory decision making.
Categories: News, Asia, Canada, Europe, US, IMDRF, In vitro diagnostics, Medical Devices, Postmarket surveillance, Regulatory intelligence, Regulatory strategy
Tags: registry data and medical devices, medical device data, approval decisions and registries