Jacqueline Mulryne

Jackie helps life science companies navigate the regulatory landscape in the EU so they can launch and keep their innovative products on the market.

She advises clients in the pharmaceutical and medical devices/MedTech 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 clinical research, authorisation, and market access. She has assisted a number of life science and medical device companies in developing and implementing cross-border regulatory action and compliance programmes.

Jackie also advises on contentious disputes in the sector, and has extensive experience in public and administrative law litigation before the national and EU Courts. In particular, she represents clients in actions arising from the decisions of regulatory bodies, such as the MHRA, the European Commission and the EMA.

She 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.