Expert opinions should raise the bar in the EU for the clinical review of high-risk devices by notified bodies, in what Gary Slack, senior vice president of the notified body at BSI Regulatory Services (Medical Devices), calls a much-needed improvement.
This is because the level of clinical scrutiny of these products by notified bodies has been “variable” in the past,...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?