Eline D'Joos
Overview
Eline D’Joos is a life sciences associate in Crowell & Moring’s Brussels office. Her practice focuses on regulatory issues and commercial transactions in the life science sector, as well as interplays with general intellectual property and data protection questions.
Career & Education
- Catholic University of Leuven, Bachelor of law, magna cum laude (best bachelor student award), 2017
- Catholic University of Leuven, Research master of law, magna cum laude, 2019
- Catholic University of Leuven, Master of education, cum laude, 2020
- Belgium
- Dutch
- English
- French
Eline's Insights
Client Alert | 6 min read | 05.12.26
EU Pharma Package: Advertising Compromise Proposal
In our ninth alert in this EU Pharma Package Series, we discussed the proposals of the Commission, Council, and Parliament with respect to advertising of medicinal products.
Client Alert | 13 min read | 05.06.26
EU Pharma Package: Interplay with the Critical Medicines Act – Status Update
Client Alert | 4 min read | 05.04.26
Decentralized Clinical Trials: Key Sponsor Considerations Under FDA and EMA Guidance
Client Alert | 11 min read | 04.27.26
The New EU "Pharma Package": Access Conditionalities and Shortage Measures Compromise Proposal
Insights
Drowning in EU regulations? Five tips for surviving the deluge of new rules
|02.03.26
Life Sciences Intellectual Property Review (LSIPR)
Will Technology Disrupt Healthcare? Navigating the Regulatory Landscape
|07.10.25
European Health & Pharmaceutical Law Review, 2025/2, p. 102-107
Critical Medicines Act : un texte décisif pour l'industrie pharma en Belgique ?
|11.07.25
La libre Belgique
Critical Medicines Act: un texte décisif pour l'industrie pharma en Belgique?
|11.07.25
La Libre Belgique
Eline's Insights
Client Alert | 6 min read | 05.12.26
EU Pharma Package: Advertising Compromise Proposal
In our ninth alert in this EU Pharma Package Series, we discussed the proposals of the Commission, Council, and Parliament with respect to advertising of medicinal products.
Client Alert | 13 min read | 05.06.26
EU Pharma Package: Interplay with the Critical Medicines Act – Status Update
Client Alert | 4 min read | 05.04.26
Decentralized Clinical Trials: Key Sponsor Considerations Under FDA and EMA Guidance
Client Alert | 11 min read | 04.27.26
The New EU "Pharma Package": Access Conditionalities and Shortage Measures Compromise Proposal




