Ranked in 1 Practice Areas
2

Band 2

Life Sciences: Regulatory

UK-wide

5 Years Ranked

About

Provided by Jacqueline Mulryne

UK

Practice Areas

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.

Chambers Review

Provided by Chambers

UK

Life Sciences: Regulatory - UK-wide
2
Band 2

Jacqueline Mulryne provides regulatory advice to pharmaceutical and medical device manufacturers. She has expertise in matters concerning orphan drugs, overseas regulation and data protection and information law with respect to life science companies.

Contributions

Latest contributions provided by Jacqueline Mulryne

Global Practice Guide
Jackie Mulryne
Ewan Townsend
Beatriz San Martin
Adela Williams
Authored by
Jackie Mulryne, Ewan Townsend, Beatriz San Martin, Adela Williams
Article • Apr 2024

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