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Diogo Geraldes, PhD MEng

Director Regulatory Strategy
Veeva Systems

Diogo is a dedicated professional with a wealth of experience in the regulatory and orthopaedic implants fields. Currently serving as the Director for Regulatory Strategy at Veeva Systems, he specializes in the EU MedTech market. Before this role, Diogo was the UKCA certification manager and a principal technical assessor at DNV, ensuring the safety and compliance of medical devices for the EU and UK markets. Diogo's career also includes work as a designer at Stryker/Stanmore Implants, where he contributed to the development of over 250 patient-specific implants, particularly focusing on complex cases in limb salvage and paediatric oncology. With a background in Biomechanics, Diogo earned his PhD at Imperial College London, where he focused on computational modelling of bone adaptation in the femur. He followed this with a Post-Doctorate at Imperial, where he developed and patented a novel glenoid implant. Diogo combines academic rigour with design, research, modelling and clinical experience in orthopaedic implants and regulatory affairs.

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