Elisabethann Wright

I specialize in EU law and regulation of pharmaceuticals, medical devices and digital

health, food supplements, functional foods, food and cosmetic products. I support clients

through the procedures and regulations necessary to place and keep their products on the

EU market through strategic advice, advocacy before institutions and agencies and

litigation before EU and EFTA courts. My experience covers the full regulatory life cycle of

products: classification of their products, establishment of a pathway to authorization, or CE

marking and promotion and marketing of their products in the EU, including related regulatory

obligations, pharmacovigilance obligations, conformity assessment of medical devices,

promotion and marketing of products including assistance in development of compliance

policies and participation in MRCs and PRCs, development of quality, supply, sales, and

services agreements, clinical trial agreements, adverse event reporting, product withdrawals,

and conduct of compliance and anti-bribery investigations.

I have been praticising in the field of Life Sciences since 1986. While is has largely been in private practice I spent four years as a Référendaire (law clerk) at the European Court of Justice and six years as a Senior Legal Officer at the EFTA Surveillance Authority.

As there is virtually nothing that I have not seen before I am able to advise clients with limited, if any, related research. This means that my response time and related costs are limited.

English, French,