I am an associate in the Regulatory, Public & Administrative Law department in our Brussels office. I advise clients on regulatory matters with a particular focus on healthcare & life sciences.
Lora specializes in regulatory and compliance advice on behalf of pharmaceutical and consumer health companies, medical technology and digital health businesses.
My area of expertise covers issues relating to life-cycle management, clinical trials, data exclusivity, product qualification / classification, to (early) market access and vigilance / pharmacovigilance. I have experience in all aspects relating to distribution and import-export, marketing, labelling, price and reimbursement authorizations, e-health together with data protection, distribution, advertising issues and product liability.
When clients seek my advice on how to conduct certain activities, I try to offer them in-depth and practical solutions rather than just offering legal advice.
My native language is Dutch and I am also fluent in English, French and Croatian.