Complete Guide to Achieving CE Certification for IVD Medical Devices in India Under EuMDR 2017/746
- Jun 22
- 3 min read
Getting CE certification for In Vitro Diagnostic (IVD) medical devices is a critical step for manufacturers in India aiming to enter the European market. The European Union Medical Device Regulation (EuMDR) 2017/746 sets strict requirements to ensure safety, performance, and quality of IVD devices. This guide offers a clear, step-by-step approach to help Indian manufacturers navigate the complex certification process and comply with EuMDR 2017/746.
