Bayode Adisa
Associate Director, Regulatory
Bayode has over 17 years' strategic and hands-on experience in the medical devices sector, including 13 years with the UK regulator of HealthTech, MHRA.
Previously, as Head of Regulatory Affairs at Real Digital International Limited, Bayode led the regulatory function for a portfolio of devices including procedure packs, specimen collection devices and kits. She oversaw registrations and post-market surveillance, while acting as the Person Responsible for Regulatory Compliance (PRRC) for the company.
At MCRA, she provided expert regulatory advice on EU and UK legislation, delivered UDI implementation strategies and helped clients meet global UDI requirements. Earlier, as Devices Data and Surveillance Strategy Manager at the MHRA, she led on UDI requirements for the future UK Medical Devices Regulations and built strategic partnerships with other government agencies, device registries and key industry stakeholders.
Bayode began her career in post-market surveillance, playing a key role in MHRA investigations into BIA-ALCL, PIP breast implants and metal-on-metal hip replacements.
She holds a BSc in Biomedical Materials Science from the University of Nottingham and an MSc in Public Health from the London School of Hygiene and Tropical Medicine.