Medical Devices

RRG provides development and regulatory advice covering all aspects of device development for both the European and US markets from clinical trials to marketing approval. We have worked on a wide variety of devices and drug-device combinations.

Services include:

  • Preparation of strategic plans
  • Evaluation of data to assess suitability for regulatory purposes
  • Identification and liaison with Notified Bodies
  • Design of Quality Management Systems
  • Clinical Trial Notifications (CTNs)
  • CE Marking
  • FDA 510K approvals

Contact Us

T: +44 (0)1276 671 166
F: +44 (0)1276 670 960

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Find Us

RRG, Innovation House
Albany Park, Camberley
Surrey. GU16 7PL

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