The Medical Device Regulatory Intelligence Center is Premier Research’s online database providing you with comprehensive and constant up-to-date EU and outside EU (OEU) country by country clinical regulatory information for medical devices. This is an excellent, easy-to-use planning tool that includes all the information you need to start-up and conduct clinical investigations in each European country with a CE market approved or non-CE marked pre-market medical device.

Access to the Regulatory Intelligence Center database is by annual subscription and will allow you to plan your medical device clinical investigations, saving you time and money while meeting your deadlines.

All information, including regulations, forms, addresses, and legal documents, is available online and is constantly updated. For further information on how you can take advantage of the most powerful and complete online medical device regulatory database available in the world, click here.