Contact Information

MedPass International SAS

95bis Boulevard Pereire 75017 Paris – France
Phone: +33 (0)1 42 12 83 30
Fax: +33 (0)1 40 53 81 11
New Business Development Department

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New EU rules on medical devices

New EU rules on medical devices to enhance patient safety and modernise public health The Commission welcomes the adoption of its proposal for two Regulations on medical devices which establish a modernised and more robust EU legislative framework to ensure better...

MEDDEV- Guidelines on Medical Devices

Issued in June 2016, raises the bar for pre and post market clinical data requirements.   MEDICAL DEVICES DIRECTIVES CLINICAL INVESTIGATION   CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC  ...

The Future Of Clinical Evidence Requirements For CE Marking

18 August 2015 Sarah Sorrel The Council of the EU’s agreed amendments to the requirements for clinical evaluation reports under the new Medical Device Regulation are substantial. And so are its proposed amendments to clinical investigations and post-market clinical...

MedPass Strategic Group – July 2015

MedPass the EU’s leading Medical Device CRO has taken another significant step in the development of its strategic group with the announcement of a number of high profile appointments. David Francis former Global Head of Active Implantable Devices at BSI, Rebecca...

Innovation Funding in France – February 2015

2015 Dear Clients, MedPass is pleased to inform you of two significant developments for the reimbursement of innovative implantable medical devices, in-vitro diagnostic solutions & medical procedures in France. A new Decree (Décret n°2015-117 du 16 février 2015)...