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The Regulatory Intelligence Center (RIC) 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.

Recent News
News  23-Jan-12 Premier Research Names Etienne Drouet Executive Director, Oncology Europe
News  16-Jan-12 Premier Research Names Dr. Colin Hayward as European Medical Director
News  11-Jan-12 Premier Research Names Susan Stansfield, PhD Executive VP, Clinical Development
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Upcoming Events
Event  03-Feb-12 ICR’s Ethics & GCP Forum
Event  28-Feb-12 ICR Symposium
Event  04-Mar-12 Partnerships in Clinical Trials Conference
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