Transcription of Clinical Data for Medical Devices - CROMSOURCE
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Clinical Data for Medical Devices - CROMSOURCE
White Paper Clinical data for Medical Devices Preparing for increased requirements in the EU Clinical data for Medical Devices March 2015 Page | 2 Table of Contents 1. Regulation of Medical Devices in the EU: on the cusp of change .. 3 2. Traditional differences between Medical device and drug Clinical studies .. 4 3. Proposal adopted by the European Parliament introduces new requirements .. 5 New device definitions introduce the concept of Clinical benefits .. 6 Failure to prove equivalence may necessitate a Clinical investigation .. 6 The range of Devices requiring Clinical investigations will be extended .. 6 Efficacy, not performance, will need to be verified in a Clinical investigation .. 7 Aim is randomised controlled Clinical trials with well-chosen controls .. 7 4. Conclusion .. 8 5. Why use a CRO? .. 9 6. How CROMSOURCE can assist .. 10 7. About the Author .. 11 8. About CROMSOURCE .. 11 Clinical data for Medical Devices March 2015 Page | 3 1.
Clinical Data for Medical Devices March 2015 Page | 3 1. Regulation of medical devices in the EU: on the cusp of change To market a medical device in the EU, a manufacturer must demonstrate that the device is safe, that
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