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Stéphane Naudin joins Qserve Group

Stéphane Naudin joins Qserve Group as a senior consultant where he is part of the medical devices team. 
Stéphane joined the global medical device team and has in-depth knowledge of European regulatory and biocompatibility requirements for non-active, implantable medical devices as well as for reusable instruments and single-use devices, especially for orthopedic and urology. Stéphane is based in Germany. 

In the industry, he worked as a developer and project manager focusing on minimal invasive instruments for various orthopedics surgical techniques, shoulder and spine implants as well as single-use devices. Stéphane also supported the development and the documentation of different medical products and worked a lot with contract test labs including biocompatibility test labs as well as many German and Swiss suppliers from metal and plastic machined as well as 3D-printed parts.

View Stéphane's personal profile to learn more about his experience and core competencies.

About Qserve Group

Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO, and quality services.

Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing to support manufacturers or distributors of medical devices and in vitro diagnostics. Check our current vacancies.
Dr. Stéphane Naudin
发布日期: 十月 05, 2022
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