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Medical Device CRO based in Europe - Medpass International

A Medical Device CRO based in Europe -MedPass International has EU Full Services of regulatory, clinical services, CE marking, market access, reimbursement.

http://www.medpass.org/

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MEDPASS INTERNATIONAL

DEJERINE SORREL SARAH

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Medpass International

Bui Pham, Cuong

95 Bis B●●●●●●●● Pereire

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Medical Device CRO based in Europe - Medpass International | medpass.org Reviews
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A Medical Device CRO based in Europe -MedPass International has EU Full Services of regulatory, clinical services, CE marking, market access, reimbursement.
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1 services
2 strategic consulting
3 clinical evaluations
4 clinical operations
5 biometrics
6 regulatory affairs
7 eu reimbursement
8 authorized representative
9 legal representative
10 expertise
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services,strategic consulting,clinical evaluations,clinical operations,biometrics,regulatory affairs,eu reimbursement,authorized representative,legal representative,expertise,cardiovascular,neurology neurovascular,oncology,ophthalmology,urology gynecology
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Medical Device CRO based in Europe - Medpass International | medpass.org Reviews

https://medpass.org

A Medical Device CRO based in Europe -MedPass International has EU Full Services of regulatory, clinical services, CE marking, market access, reimbursement.

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medpass.org medpass.org
1

ROUTE TO MARKET STRATEGIES - MedPass International MedPass International

http://medpass.org/medical_regulatory_clinical_reimbursement

ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. MedPass assists companies in developing integrated, regulatory, clinical and reimbursement strategies for Europe much appreciated by life science investors and early stage companies. Selection of and liaison with Notified Bodies. Clinical trial strategies for CE marking and reimbursement. Risk management for major adverse events.

2

PUBLICATIONS Archives - MedPass International MedPass International

http://medpass.org/category/publications

ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. The Future Of Clinical Evidence Requirements For CE Marking – August 2015. 8211; The Future Of Clinical Evidence Requirements For CE Marking – Sarah Sorrel. Clinical Evaluation Plan – DeviceMed. 8211; Clinical Evaluation Plan. The Medical Device price. 8211; The Medical Device price. Policy & Regulation Lessons to be learned courtesy of PIP. 8211; Policy and Regulation Lessons to be learned courtesy of PIP – Jeremy Tinkler.

3

CLIENT EXPERIENCES - MedPass International MedPass International

http://medpass.org/client-experiences

ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. I want to thank you for your incredible efforts as we collect our interim 30 day and 6 Month Data! Director of Clinical Affairs, USA. Director of Clinical Research, USA. Just Fantabulous effort to accomplish this turnaround and submit the revised plan. To all the team and Medpass really big THANK YOU! President and CEO, USA. President and CEO, USA. Yes it was a pleasure working with the MedPass team; you are all true professionals!

4

MEDICAL DEVICE EXPERTISE - MedPass International MedPass International

http://medpass.org/medical_device_expertise

ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. Transcatheter heart valve replacements. Artificial heart valves (surgical). Heart valve repair systems. Left Ventricular Assist devices. Robotic surgical systems for coronary bypass surgery. Ultrasound devices to enhance thrombolytic therapy. Pleural sealant systems for thoracic surgery. Pulmonary artery pressure measurement devices. Coronary sinus pressure management devices. Guidewires for peripheral total occlusions. Robotic su...

5

MedPass Careers offers MedPass International

http://medpass.org/medical_careers

ROUTE TO MARKET STRATEGIES. AUTHORIZED / LEGAL REP. MARKET ACCESS / REIMB. Regulatory Affairs Associate – Medical Devices. MedPass International is a consulting firm specialising in the regulation and clinical development of new medical technologies. Founded in 1991 and located in Paris, MedPass International provides a full range of customised regulatory/reimbursement consulting and CRO services to medical device manufacturers seeking to place and maintain their products on the European market. Knowledg...

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EAAR | Members

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European Commission Working Groups. Email: t.pennings@cepartner4u.com. Donawa Lifescience Consulting s.r.l. Medical Device and QA Services Ltd. Medical Device Safety Service GmbH. Medical Technology Promedt Consulting GmbH. Email: medpass.ar@medpass.org. Obelis s.a. European Authorized Representative Center. Qarad European Regulatory Services. Tecno-Med Ingenieros S.L. EC WG – CIE. EC WG – EUDAMED. EC WG – IMDRF. EC WG – IVD Technical. EC WG – MDEG on B&C. EC WG – N&ET. EC WG – NB-MED.

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Medical Device CRO based in Europe - Medpass International

Orthopaedics – Spine. Endovascular – Peripheral Vascular. GI Tract – Liver. MedPass International is the leading Europe Medical Device CRO,Regulatory and Reimbursement Consultancy specialized, in medical device development and market access. A Medical Device CRO, Regulatory and Reimbursement Consultancy. Helps companies worldwide bring new technologies to the market by providing a full range of services in medical device development. Key areas of focus include:. Will be implemented in 2020 which will pro...

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Medpassion Hamburg | Medizinische Exzellenz

Medpassion Hamburg ™. Allgemeinmedizin - Zahnmedizin - Schönheitschirurgie. Medizinische Exzellenz in Hamburg Winterhude. Medpassion™ bietet Ihnen als Patient ein außergewöhnliches Praxis-Umfeld und eine medizinische Betreuung auf höchstem Niveau. Die medizinischen Leistungsbereiche von Medpassion™ umfassen allerneueste Therapie- und Behandlungsmethoden, modernste Diagnostik-Systeme und innovative Technologien. Medizinscher Vorsprung durch Innovation und Leidenschaft. Juli 8th, 2015. Medpassion-Hamburg&#...