Eucomed Q&A: Where Do EU Regs Get It Right? An Emphasis On Innovation
This article was originally published in The Gray Sheet
Executive Summary
With U.S. medical device regulatory reforms looming, comparisons between the U.S. and European systems have become popular talking points in the debate over where FDA should be heading.
You may also be interested in...
Cardiologist Group Calls For Centralized Device Oversight In Europe
The European Society of Cardiology says medical device oversight in Europe is not sufficient, and is calling for a single European regulatory body to oversee product evaluation and approval.
Cardiologist Group Calls For Centralized Device Oversight In Europe
The European Society of Cardiology says medical device oversight in Europe is not sufficient, and is calling for a single European regulatory body to oversee product evaluation and approval.
Global Harmonization Task Force To Disband As Focus Shifts To Implementation
The Global Harmonization Task Force as currently formed will disband and be replaced with a new, regulators-only forum focused on implementing harmonized policies across the globe, participants say.