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Fabien Roy

Fabien Roy

Brussels, Brussels    Belgium
Quality Management
Quality Management, Medical Device,...More
Spoken at 2 events

Biography :

Fabien focuses particularly on guiding clients through the regulatory and technical regulatory requirements applicable to the CE marking of medical devices. Fabien is also a qualified lead auditor for ISO 13485 quality management systems. He consequently has a deep understanding of the range of quality issues encountered by medical device Clients.

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Specialties

Quality Management

Interested Topics

Quality Management, Medical Device, Regulatory Affairs, Pharmaceutical Industry, Clinical Research, Clinical Trials, Biotechnology, Pharmaceuticals, Life Sciences, Healthcare Management

State Licenses

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Board Certifications

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Professional Association

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Languages

English, French

Conference Session Materials

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MOC / CME / CE Requirements
Virginia Board of Medicine

Virginia Board of Medicine accepts the courses that are endorsed by ACCME and grants AMA PRA Category 1 credit.

MD/DO Requirement:

CME Credits Required : 60.00 | Licensing Cycle AMA PRA : 2 Years | Category Credits : 30.00

MD-

DO-

  • 60 hours of CME for every 2 years followed by immediate preceding renewal
  • A minimum of 30 hours must be under Category 1, of which 2 hours must be in pain management, proper prescribing of controlled substances, and the diagnosis of management of addiction.
  • OCC/MOC is not specifically addressed, but an endorsement of recertification by a specialty board is admitted as a substitute by the Virginia Board of Medicine.