SelienCoolen

Associate

Amsterdã + 31.20.305.4286

Selien Coolen advises clients on EU and national regulatory matters in the health care and life sciences area, including medical devices, biotechnology, pharmaceuticals, and food and cosmetics. She provides comprehensive guidance across the full life cycle of medical products — from pre-market authorizations and conformity assessments to marketing, distribution, and post-market compliance. Selien also conducts regulatory and compliance analyses for life sciences M&A transactions.

​In addition to her regulatory practice, Selien represents clients in corporate litigation and civil proceedings, including appearances before the Enterprise Chamber of the Amsterdam Court of Appeal. Her experience covers complex commercial disputes, shareholder disputes, directors' and professional liability, contract law, and disputes related to breach of contract, tort, and damage claims.

Selien is an active member of the Dutch Association for Health Law (VGR).

​Prior to joining Jones Day in 2015, Selien worked as a court clerk at the Civil Department of the Court of Maastricht and the Court of Amsterdam.

Experiência

  • Eurobio Scientific acquires GenDxJones Day advised Eurobio Scientific SA in the acquisition and financing of the Dutch company Genome Diagnostics BV (GenDx) from its founder and its shareholders for €135 million (net of adjusted cash).