​Christian has over 25 years of experience in the medical device industry. With a PhD in materials science and a Master’s degree in biomedical engineering, he combines scientific rigor with practical insight across product development, clinical studies, regulatory affairs and quality systems.
He has developed strong expertise in biological evaluation, including the preparation of Biological Evaluation Plans and Reports (BEP/BER), toxicological risk assessments, and biocompatibility strategies aligned with ISO 10993.
He is also highly experienced in CE marking documentation, particularly in writing Clinical Evaluation Reports (CERs), and has applied MDR requirements extensively through his role as Director of Quality & Regulatory Affairs in a MedTech SME.
With a versatile yet specialized profile, Christian brings clarity and confidence to your regulatory journey — you're in good hands.

​Jean-François has more than 30 years of experience in medical devices. Trained as an engineer, his expertise covers product development, clinical research and quality assurance. His therapeutic knowledge includes orthopedics, spine, neurology, cardiology, and others, for devices from class I to III.
Trained on technical and scientific excellence in large groups and with practical experience in start-ups, he has particular expertise in risk management, QMS implementation and audit, scientific literature review and post-market clinical follow-up (PMCF). Over the last few years, he has developed an original platform for multiple post-market clinical studies, providing significant contributions to Clinical Evaluation Reports (CERs) or reimbursement files.