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Fabian Huber advises and represents national and international clients comprehensively in the field of pharmaceutical and medical devices law, including regulatory, compliance, liability and competition law. Fabian Huber acts as an advisor and litigator. Fabian Huber joined Preu Bohlig & Partner’s Munich office as a lawyer in 2024, having previously worked in major international law firms and the biotech industry.
University Regensburg | Ludwig-Maximilians-University Munich | University Augsburg | Doctorate at University Augsburg | LL.M. at Heinrich-Heine-University Dusseldorf | Legal clerkship in the OLG district of Munich
Medical Law Working Group of the German Bar Association e.V.
Concept of Medical Research and Distinction from Therapy in Spickhoff/Handorn, Handbook on Medical Research, 2024, C.H. Beck Verlag
Cloth mask not a medical device – note dispensable (together with Kendziur), GRURPrax 2021, 35
Decision on advertising of digital medical consultations by Swiss-based doctors (together with von Nussbaum), International Law Office, 2020
Advertising of digital medical consultations by Swiss-based doctors (together with von Nussbaum), GRURPrax 2020, 431
Binding implications of notification under German Drug Act and qualification of preparation as presentation drug, International Law Office (with Kendziur), 2020
Distribution of a preparation approved as a medical device as a presentation drug (together with Kendziur), GRURPrax 2020, 394
Compulsory licensing under Infection Protection Act: effects on data exclusivity under pharmaceutical law, International Law Office (together with von Nussbaum), 2020
Medical device law transposition act: sanctions under chapter 9, MPR 2020, 89
Regulation of medical marijuana, International Law Office (with von Nussbaum), 2020
Granting of gifts by pharmacies, International Law Office (with von Nussbaum), 2019
MDR and medical software: insurance under German law (with von Nussbaum), International Law Office, 2019
MDR and medical software: liability under German law (together with von Nussbaum), International Law Office, 2019
OEM/PLM designs under the MDR: recommendations for action in practice, MPR 2019, 195
Software as a medical device: liability and insurance law aspects (together with Jakobs), MPR 2019, 1
