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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
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NEWS

HAS Event

Amélioration de la qualité de vie des patients et accès à l’innovation : deux priorités dans les évaluations des dispositifs médicaux – 24 novembre 2017...

National Health Strategy

La ministre de la Santé, Agnès Buzyn, a lancé ce lundi une grande concertation autour de la stratégie nationale de santé (SNS) qui sera adoptée en décembre par décret et fixera les priorités et les objectifs pour cinq ans. « L’objectif est de développer une...

SNITEM: 3 New Leaflets Published

A l’occasion des 5èmes Rencontres du Progrès Médical, le Syndicat National de l’Industrie des Technologies Médicales (SNITEM) annonce la parution de trois nouveaux livrets : la santé de la femme, la contactologie et les pathologies veino-lymphatiques. Véritable état...

Endometriosis: diagnosis and management

This guideline covers diagnosing and managing endometriosis. It aims to raise awareness of the symptoms of endometriosis, and to provide clear advice on what action to take when women with signs and symptoms first present in healthcare settings. It also provides...

A new era of data protection is beginning

“A new era of data protection is beginning. For medical device companies, compliance must begin promptly  in order to comply with the new Data Protection Regulations. The European Union’s General Data Protection Regulation (GDPR – 2016/679) was published on April 27,...

New Regulation in the Official Journal of the EU

New Medical Device Regulation (MDR) have been published in the Official Journal of the EU on May 5, 2017 The new regulation on Medical Devices (EU) 2017/745 was published on May 5 and will take effect from May 25, 2017. The transitional period will officially start...

New Medical Device and In Vitro Diagnostic

New Medical Device and In Vitro Diagnostic Medical Device Regulations (MDR & IVDR) have been published in the Official Journal of the EU on May 5, 2017 The new regulation on Medical Devices (EU) 2017/745 and on In Vitro Diagnostic Medical Devices (EU) 2017/746...

Loi Jarde

Latest DeviceMed publication  LOI JARDE – By Amélie Archer & Lucile Bernard – , MedPass International Link below AFCROs2 – Loi...

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)...