Jacqueline Mulryne BA, MA

Jackie Mulryne advises clients in the life sciences, medical devices, cosmetics and foods sectors, and has a broad practice providing regulatory compliance and public policy advice. She advises on UK and EU law, and has experience with a range of regulatory issues that arise throughout the product life cycle, including borderline classification, clinical research, authorisation, advertising and labeling, and pricing and reimbursement. She has assisted a number of life science and medical device companies in developing and implementing cross-border regulatory action and compliance programmes.

Ms. Mulryne also advises on contentious disputes in the sector, and she has extensive experience in public and administrative law litigation before the national and EU Courts. She advises on actions arising from the decisions of regulatory bodies, such as the Medicines and Healthcare products Regulatory Agency (MHRA), the European Medicines Agency (EMA), the National Institute for Health and Care Excellence (NICE) and the Cancer Drugs Fund (CDF), and represents clients challenging public procurement tenders under EU and UK rules. Ms. Mulryne also works on product liability matters on behalf of pharmaceutical and medical device companies, and has assisted on large multiparty actions, and in defending individual personal injury and product liability claims. Ms. Mulryne is committed to pro bono work, and has advised a variety of clients on the protection of human rights and the right to a fair trial. She has also spent time working for the Cambodian Center for Human Rights in Cambodia.