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Svitlana Marchand
Regulatory Affairs Project Manager at Medpass International
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Work Experience
Regulatory Affairs Project Manager
Dec 2017 - Present · 7 years
Clinical Project Leader
Nov 2011 - Dec 2017 · 6 years and 1 months
verum staticon
Junior Local Project Manager
Jan 2009 - Feb 2011 · 2 years and 1 months
Company Details
11-50 Employees
Specialists in Clinical Development, Regulatory Strategies and EU Market Access for Medical Devices. MedPass International is your Partner in the EU for medical devices Regulatory, Reimbursement and CRO Services. MedPass is built on the concept of being a “one stop shop” for medical device manufacturers seeking access to the EU market by offering a full range of services: -Strategic consulting, -CRO services, -Biometrics services, -Regulatory affairs, -Access market Pricing and reimbursement, -Authorized representative
Year Founded
1991
Social Media
Linkedin
Industry
Medical Device, Medical imaging equipment and instruments, Medical Equipment, Health, Medicine and surgery - apparatus and equipment, Herb Medicine, Health Medical
HQ Location
95 bis boulevard Pereire Paris, 75017, FR
Keywords
EU Medical device CRORegulatory affairsStrategic consultingBiometrics services
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