Her experience covers the full regulatory life cycle of products: classification of their products, establishment of a pathway to authorisation and marketing of their products in the EU (including related regulatory obligations), pharmacovigilance obligations, conformity assessment of medical devices, promotion and marketing of products, sales agreements, clinical trial agreements, adverse event reporting, product withdrawals, data privacy obligations, and conduct of compliance and anti-bribery investigations. In recent years she has advised clients and published extensively on digital health issues, such as their implications for CE marking obligations for medical devices, and obligations for life sciences companies related to collecting and processing personal health data under the GDPR. 

Elisabethann has substantial experience in litigation before the European Court of Justice, the European Court of First Instance, and the European Free Trade Agreement (EFTA) Court, including challenges, on behalf of industry clients, to decisions of EU institutions and the validity of EU legislation. Elisabethann was a Référendaire (Law Clerk) at the Court of Justice of the European Communities for several years.

Elisabethann is recognized as a leading practitioner in the field by Chambers Europe, Legal 500, Best Lawyers in Belgium, Who’s Who Legal, and Acritas Stars.