Mateusz Mądry
Partner at DZP
Speaker

Profile

Head of Life Sciences Practice.
Expert in both national and international law regarding pharmaceuticals, medical devices and innovative technologies.
Mainly advises life sciences entities on regulatory requirements, market access, and competition and compliance issues.
Represents clients in proceedings before administrative authorities, particularly the Minister of Health and units subordinate to the Minister, and also at the stage of court control of decisions.
In the years 2014-2016, he worked in the legal department of the European Medicines Agency, where he co-created EU regulatory practice and soft laws for the life sciences sector. He has represented Poland at the European Commission in working groups and standing committees.
For many years, he also gained experience in domestic administration at the Ministry of Health and the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, where he held various positions, including department director.
Author and co-author of numerous publications on pharmaceutical law, including a commentary on the Reimbursement Act.
Member of the Warsaw Bar Association.