Device Surveillance Reform Board Looks To Add Small-Firm Experience
This article was originally published in The Gray Sheet
Executive Summary
The public-private National Medical Device Evaluation System Planning Board, first convened in 2014, is seeking nominations for new members to support the next two-year phase of development of a revamped postmarket surveillance system.
You may also be interested in...
Postmarket Surveillance Reform Board Gets Injection Of Device Industry Experience
The appointments of three device industry veterans to the Brookings-administered, and partially FDA-funded, Planning Board is intended to expand the range of input in the next phase of development of a new National Medical Device Surveillance System.
Task Force Advocates Making Registries Better Than Sum Of Their Parts
The FDA-endorsed Medical Device Registry Task Force maps out a path toward "coordinated registry networks," starting with pilot projects and 11 prioritized device categories.
Planning Board Proposes Postmarket Device Surveillance Timeline
A planning board created to develop a framework for a new U.S. medical device surveillance system has proposed a seven year plan on how to get the system up and running, which will include creating incentive systems for stakeholders as well as reducing the burden of recording and managing device data.