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Susan Partridge, PhD

Clinical Regulatory Lead
BSI
Leeds, England, United Kingdom

Susan Partridge is a Clinical Regulatory Lead at BSI with over 15 years’ experience in the orthopaedic medical device industry. She has presented at key regulatory conferences and collaborated on BSI white papers on topics such as investigator-initiated studies, early feasibility studies, state of the art, MDR clinical evidence requirements and Article 61.10. She has performed clinical evaluation assessments as part of the Orthopaedic & Dental team at BSI and written clinical evaluation reports for various classes of orthopaedic devices in industry. She has a PhD in medical engineering and an academic research background, which included clinical research, lecturing in biomechanics and pre-clinical testing of joint replacements. She has also been a member of an NHS Research Ethics Committee for the last 9 years.

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