Our team is located throughout France
Based in various regions, our consultants provide services throughout France—either in person or remotely—to support manufacturers, distributors, importers, authorized representatives, and subcontractors of medical devices and in vitro diagnostic medical devices.
This close relationship allows us to offer responsive, personalized support tailored to each client’s needs, regardless of the size of their business or the stage of development of their systems.
Tours
Catherine BACOU
President of Isocèle Médical
Qualification
- Master's Degree in Mathematics and Physics
- IRCA Quality Auditor
Experience
- 20 years of professional experience in the corporate sector in management and executive positions
- Over 25 years of experience in quality and regulatory affairs consulting for the medical device industry
Auvergne-Centre Region
Fanny MARILLER
Chief Executive Officer
Qualification
- Master II in Quality Management
- University Certificate in Regulatory Affairs for Medical Devices
Experience
- Over 15 years of experience in quality and regulatory affairs consulting for the medical device industry
Southwest Region
Raphaël MOUSTIE
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Master II in Biotechnology Applied to Health
- Master's in Quality
- ISO 13485 Lead Auditor
Experience
- Over 15 years of experience in quality and regulatory affairs consulting for the medical device industry
Rhône-Alpes Region
Caroline CREUSOT
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Master's in Quality, Safety, and Environment Management
- University Certificate – Regulatory Affairs for Medical Devices
- ISO 13485 Lead Auditor
Experience
- Over 10 years of experience in quality and regulatory affairs consulting for the medical device industry.
Ile-de-France Region - Paris
Stéphane WEHRLI
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Agricultural Engineer, ENSAIA (Nancy)
- University Certificate – Regulatory Affairs for Medical Devices
- ISO 13485 Lead Auditor
Experience
- Over 10 years of experience in quality and regulatory affairs consulting for the medical device industry
Northeast Region
Anne-Cécile SCHWARTZ
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Master 2 in Pharmaceutical Sciences, Regulatory Affairs and Pharmaceutical Law track, with a specialization in Medical Device Regulation
- University Diploma in Public Health, with a focus on Epidemiology, Clinical Research, and Evaluation,
- University Certificate in Clinical Research Methods
- ISO 13485 Lead Auditor
Experience
- Over 10 years of experience in quality and regulatory affairs consulting for the medical device industry
Occitanie–PACA Region
Martin BROCHU
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Master's in Health Biology
- Master's in International Regulatory Environment for Healthcare Companies and Products
- ISO 13485 Lead Auditor
Experience
- Over 15 years of experience in quality and regulatory affairs consulting for the medical device industry
Ile-de-France Region - Paris
Estelle MORFIN
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Master's in Medical Device Regulatory Affairs
- Engineer, Biomedical Engineering – Franche-Comté Higher Institute of Engineering
- ISO 13485 Lead Auditor
Experience
- Over 10 years of experience in quality and regulatory affairs consulting for the medical device industry
Northwest Region
Nancy TRICHEREAU
Quality and Regulatory Affairs Consultant – Medical Devices
Qualification
- Bachelor's and Master's Degree I in Biotechnology
- AFNOR Training: Internal and External Auditor
- Animal Origin Auditor
Experience
- Over 20 years of experience in quality and regulatory affairs consulting for the medical device industry