Samir Benallel possesses extensive experience in regulatory affairs within the medical technology field, having worked at notable companies such as Zimmer Biomet and ZEISS Medical Technology. With a background as Chargé d'Affaires Réglementaires and Regulatory Affairs Manager, Samir has been involved in CE marking documentation, project management, regulatory compliance, and international registration processes. Currently serving as a Senior Independent Consultant at S.B.M and an Auditor for ISO standards, Samir's expertise includes risk management documentation and support for various projects. Educational qualifications include a Bachelor's degree in Biochemistry and a Master's degree in Biomaterials & Medical Devices from the University of Bordeaux.
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