Regulation (EU) 2017/746 (IVDR) | MDR IVDR Amendment | OMC Medical Limited

Omcmedical24 Jan, 2024Health

Regulation (EU) 2017/746, also known as the In Vitro Diagnostic Regulation (IVDR), signifies a pivotal regulatory framework governing medical devices in the European Union. The MDR IVDR Amendment reflects the continuous efforts to enhance and adapt regulatory standards in the dynamic field of in vitro diagnostics. OMC Medical Limited, as a key player in the industry, adheres to these regulations, ensuring the safety, quality, and efficacy of their medical devices. This harmonized approach underscores the commitment to advancing healthcare standards and fostering innovation in the European market.