Alison Wilson BSc, MSc

Alison is an independent regulatory affairs consultant. Previously regulatory affairs manager for Smith & Nephew Wound Management, she has 30 years’ experience of regulatory affairs in medicinal products, human tissue products and medical devices. She is a nominated UK expert for ISO (International Standards Organisation) TC150/WG 11 - Tissue Engineered Medical Products and a member of the British Standards Insititute (BSI) Technical Panel RGM/1 – Regenerative Medicine. As a member of RGM/1, which works to ensure a high level of representation and support for the UK and EU within the international standards community, Alison is closely involved in the development of new documents and guidelines for regenerative medicine and advanced therapies.

Alison has a MSc in stem cell biology and regenerative medicine. She is a Fellow of The Organisation for Professionals in Regulatory Affairs (TOPRA). She is part of the Module delivery team for the TOPRA MSc in Regulatory Affairs (Module 9 – Biotechnology) and was Module Advisor for the MSc in Medical Technology Regulatory Affairs (Module 6 – Combination Products and Other Technologies) from 2006-2012.