Mr. Olsen is a senior Quality and Regulatory professional with 35 years of diversified experience in the device industry. Russ previously served as VP of QA/RA and Engineering for Stanmore Implants in the UK and prior to that was the VP of QA/RA for Mindray DS USA Inc. Russ’s device experience includes orthopaedic implants and capital equipment, most notably, Intra-Aortic balloon pumps, Patient Monitoring devices, Diagnostic Ultrasound, and Anesthesia delivery systems. Russ has significant Regulatory and Quality experience in the US, Canada, and Europe. He has developed and implemented Quality Systems to meet the US and global requirements. Russ has successfully led numerous regulatory body inspections in the US and in Europe. He has cleared numerous class II and class III devices through the FDA, Health Canada and CE marking process.
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