UK Law and Practice Contributed by: Jackie Mulryne, Ewan Townsend, Adela Williams and Libby Amos-Stone, Arnold & Porter
Arnold & Porter is an international law firm at the intersection of business, law and regulatory policy, serving clients whose business needs require expert US and/or European cross-bor- der regulatory, litigation and transactional ser- vices. The firm has a particularly high reputa- tion for advising on UK and EU law relating to pharmaceuticals, biotechnology and healthcare
products and medical devices, and for assist- ing clients in interpreting and complying with the regulatory framework that surrounds these products. The authors would like to acknowl- edge the contributions of Eleri Abreo, Chris- topher Bates, Katya Farkas, Sofia Holmquist, Heba Jalil and Joy Wee.
Authors
Jackie Mulryne is a regulatory and litigation partner at Arnold & Porter who advises clients in the life sciences and medical devices sectors. She has a broad practice providing
Ewan Townsend is a partner at Arnold & Porter who specialises in transactional and regulatory work in the life sciences sector. He has experience in drafting and negotiating a wide range of
regulatory compliance and public policy advice. She is highly experienced in a wide range of regulatory issues that arise throughout the product life cycle for both medicinal products and medical devices. She also advises on public and administrative law cases brought before the UK and European courts, arising from the decisions of regulatory bodies in the EU (EMA and Commission) and the UK (MHRA).
complex, high-value agreements, such as licences and collaboration agreements, manufacture and supply agreements, technology transfers and clinical trial agreements. He is uniquely placed in his ability to advise on the regulatory issues that arise in the context of those transactions, particularly in relation to marketing authorisations, manufacturing and distribution, pricing, advertising and promotion, freedom of information and data protection.
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