Medical Device Management assists clients to bring medical devices to market, helping you to achieve CE marking, FDA listing or support you with other geographic applications. We provide project management, design, product testing, quality systems, technical files and regulatory compliance. All of our services are certified by BSI to EN ISO 138485:2016
Whether you want to bring a new product to the market or just want to upgrade your technical documents to the new requirements of the Medical Device Regulations we can help you.
Exhibitor Data Sheet