Medical Device EU

The Medical Device EU plugin provides access to all relevant guidances, regulations, and requirements in the European medical devices field. It is a valuable resource for anyone seeking information on European regulations, including the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). The plugin covers topics such as regulatory affairs, compliance assistance, simplifying the regulation landscape, and provides expertise in medical device regulatory affairs. It also includes information on classification rules, ISO standards, technical documentation, and guidelines. Whether you need assistance with regulatory compliance, understanding the transition provisions, or navigating the regulatory landscape, this plugin is a helpful tool for medical device professionals.