Mathias Klümper, Ph.d.

Mathias Klümper worked in the Düsseldorf office of Clifford Chance in the “Healthcare, Life Sciences and Chemicals” industry group as of 2004. He has been a partner in our firm since 2008.

He mainly advises clients from the pharmaceutical and medical technology sectors on legal issues typical of the industry, such as clinical trials, drug advertising law and product liability. In this context, he represents a large number of companies in drug advertising and product liability proceedings before German courts.

In addition, he advises international companies on questions of market access and market entry with medicinal products and medical devices in Germany and, in this context, also helps foreign companies to establish a branch in Germany. In recent years, he has also been increasingly involved in digital topics such as software as a medical device (SaMD), digital health applications (DiGA) and artificial intelligence and their impact on the work of pharmaceutical and medical device companies.

Mathias Klümper is not only familiar with the legal perspective, but has also gained experience as in-house counsel in several interim management positions in the legal departments of international pharmaceutical and medical device companies.

In addition, he has been a lecturer at the University of Marburg since 2015 as part of the Master’s program in Pharmaceutical Law (LL.M. Pharmaceutical Law).

He was a board member of the German Society for Pharmaceutical Medicine e.V. (DGPharMed e.V.) from 2013 – 2015 and is a founding member of the DGPharMed’s “Digital Health” department, which has existed since 2024.

He has also been a member of the Compliance Advisory Board of the Self-Regulatory Association for Pharmaceuticals and Cooperation in Healthcare (AKG e.V.) since 2012 and is a regular speaker at compliance officer training courses.

Mathias Klümper is the author of various publications, such as co-author of the “Handbuch Pharmarecht!” (Pharmaceutical Law Handbook), editors: Anhalt/Dieners, the “Vertragshandbuch Pharmarecht” (Pharmaceutical Law Contract Handbook), editors: Stief/Bromm and the “Leitfaden klinische Prüfungen Arzneimittel und Medizinprodukte (Clinical Trials Guidelines for Pharmaceuticals and Medical Device), editors: Sickmüller/Gleiter/Hinze, as well as a regular author in specialist journals on pharmaceutical and medical device law.

Languages: Deutsch and Englisch

Tel: 040 / 180 248 92 – 0
Fax: 040 / 180 248 92 – 9