Full Name
Jeremy Tinkler
Job Title
Member, EAAR / Director, Regulatory Consultancy & QA
Company
ICON
Speaker Bio
A European Registered Toxicologist, Jeremy spent 10 years in general toxicology in laboratories and the UK Health and Safety Executive before joining what is now MHRA, working there for 20 years. He then joined MedPass International, a clinical research organisation and regulatory consultancy based in Paris, which, in 2020, was acquired by ICON, the world’s largest clinical research organisation.
His move into medical devices led to experience in all aspects of their regulation. He has written a textbook on biocompatibility and many publications or presentations on various aspects of device safety and regulation. He has 35 years’ experience writing standards and regulatory guidance in biological safety, risk management, clinical investigation and evaluation (including MEDDEV 2.7/1), heart valves, breast and other implants, and tissue engineering. Since 2018 he has been Chair of the ISO Technical Committee responsible for developing international standards in biological and clinical evaluation and tissue safety.
His move into medical devices led to experience in all aspects of their regulation. He has written a textbook on biocompatibility and many publications or presentations on various aspects of device safety and regulation. He has 35 years’ experience writing standards and regulatory guidance in biological safety, risk management, clinical investigation and evaluation (including MEDDEV 2.7/1), heart valves, breast and other implants, and tissue engineering. Since 2018 he has been Chair of the ISO Technical Committee responsible for developing international standards in biological and clinical evaluation and tissue safety.
Speaking At
