Elinor Pecsteen advises international clients on a wide range of EU and national regulatory matters. Her practice focuses on life sciences, particularly the medical device, pharmaceutical, biotechnology, cosmetics, and food sectors. She also advises clients on general EU product regulation in relation to EU labeling, marketing obligations, and product safety.
Elinor assists clients on matters involving the full life cycle of products, from pre-market authorizations and conformity assessments to post-market issues, including advertising, distribution and compliance with anti-bribery/sunshine requirements, and data privacy.
Prior to being in private practice, Elinor worked for a year at the European Food Safety Authority.
Guidance for European MA Holders to Prepare for Brexit, Pharmaceutical & Medical Device Update, Vol. IV, Issue III
- College of Europe, Bruges (LL.M. in EU Law cum laude 2015); Katholieke Universiteit Leuven (LL.M. in EU & International Law cum laude 2014); Facultés Universitaires Saint-Louis (LL.B. 2012)
- Brussels Bar
- Trainee, European Food Safety Authority, Parma, Italy (2015-2016)