Global Medtech Guidance Tracker: March 2022
Executive Summary
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Thirty documents have been posted on the tracker since its last update.
You may also be interested in...
European Commission Adds To Advice On High Risk Device Safety And Performance Requirements
The European Commission’s MDCG has issued revised guidance and advice on safety and clinical performance data required for implantable and class III devices under the MDR.
Recalls 101: New FDA Guidance Gives Basic Advice On Prepping For, Executing A Recall
The US FDA’s final guidance is a basic how-to guide for manufacturers to prepare for and roll out a product recall action.
Singapore To Require GMP Evidence On Chemical Substance Drug Manufacturers
Singapore is taking steps to align good manufacturing practice requirements for chemical and biologic drug substance manufacturers and has rolled out a one-year transition plan for compliance.