- Specializes in administrative law, in particular pharmaceutical and medical device law, with a focus on the regulatory and administrative proceeding areas.
- Represents clients in administrative proceedings and administrative court proceedings and provides ongoing advice throughout the lifecycle of products marketed by pharmaceutical and medical device industry clients.
- Experienced in projects involving drafting new regulations and helping clients comply with existing regulatory requirements.
- Supports clients in the comprehensive implementation of internal compliance systems and quality and risk management systems.
- He is a certified ISO 13485:2016 Quality Management System Internal Auditor.
- Member of the Wrocław Bar Association of Attorneys-at-Law.
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DZP ranks top in international ranking - Legal 500 EMEA 2025 results
News | 26.03.2025
In the latest ranking published by Legal 500, 18 DZP experts were highlighted as leading lawyers, and as many as 10 new lawyers were recognized by this prestigious ranking.
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MIT Global Startup Workshop 2025
Event | 24.03.2025
Mateusz Mądry, Marek Paluch, and Maciej Zajda will participate in the conference organized by the Massachusetts Institute of Technology, which will be held in Poland for the first time.
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Top Trends Life Sciences 2025 Report
News | 12.03.2025
Our experts have prepared a report summarizing the key issues discussed at the DZP conference on upcoming regulatory changes and challenges in the pharmaceutical industry.
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Supporting young founders: DZP – content partner of the Innovations Hub Foundation's Mentoring Programme
News | 19.06.2024
As part of the cooperation with the Innovations Hub Foundation, DZP's lawyers have advised on the legal issues of the emerging startups participating in the project.