Claudia Vimercati Email & Phone Number | I am a biomedical engineer with relevant working experience in the field of the medical devices since 2007. Currently I’m product assessor for medical devices CE certification, reviewer of technical file according to MDD 93/42 and MDR 2017/745 (MDN 1202 and 1203). I’m auditor and lead auditor for CE, ISO 13485 and ISO 9001 too. My previous experience consists in 13 years of vascular devices Research and Development, starting as R&D engineer to R&D Program Manager. I reached a comprehensive knowledge in product development, from the idea design stage to the worldwide submissions for certification and market release and in product changes. I've worked on complex multi-site projects for different peripheral vascular devices: PTA (percutaneous transluminal angioplasty) devices, CTO (chronic total occlusions) devices, EPD (embolic protection devices), DCB (drug coated balloon) devices. My background includes multiple classes in the field of engineering, soft skills and clinical and congresses attendance. My education is significant as well, since it includes, after a master degree in Biomedical Engineering @ Politecnico of Milan, a II level master degree in Engineering in Surgery in which I had the opportunity to directly learn from different surgeons in the operating room.

Claudia Vimercati

I am a biomedical engineer with relevant working experience in the field of the medical devices sinc...
Florence, Florence, Italy

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Claudia Vimercati’s Location Florence, Florence, Italy

Claudia Vimercati’s Current Industry Tuv Rheinland Europe

Claudia Vimercati’s Prior Industry Medtronic

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Medical Devices Project Manager

2021-02-01T00:00:00.000Z - Present

R&D Program Manager at Medtronic Peripheral Vascular

2016-01-01T00:00:00.000Z - 2020-12-01T00:00:00.000Z

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Claudia Vimercati is a I am a biomedical engineer with relevant working experience in the field of the medical devices since 2007. Currently I’m product assessor for medical devices CE certification, reviewer of technical file according to MDD 93/42 and MDR 2017/745 (MDN 1202 and 1203). I’m auditor and lead auditor for CE, ISO 13485 and ISO 9001 too. My previous experience consists in 13 years of vascular devices Research and Development, starting as R&D engineer to R&D Program Manager. I reached a comprehensive knowledge in product development, from the idea design stage to the worldwide submissions for certification and market release and in product changes. I've worked on complex multi-site projects for different peripheral vascular devices: PTA (percutaneous transluminal angioplasty) devices, CTO (chronic total occlusions) devices, EPD (embolic protection devices), DCB (drug coated balloon) devices. My background includes multiple classes in the field of engineering, soft skills and clinical and congresses attendance. My education is significant as well, since it includes, after a master degree in Biomedical Engineering @ Politecnico of Milan, a II level master degree in Engineering in Surgery in which I had the opportunity to directly learn from different surgeons in the operating room.