Pharmaceutical Law | Professional literature for training, studies and practice

In the Pharmaceutical Law category, you will find comprehensive professional literature on the legal framework governing drug development, approval, marketing, and liability. The works address key topics such as the German Medicines Act (AMG), patent protection, clinical trials, data protection in research, pricing under the AMNOG procedure, and liability issues related to off-label use. Additionally, they cover intersections with related legal fields such as medical device law, pharmaceutical advertising law, and pharmaceutical law in an international context.

The selection includes commentaries, handbooks, practice-oriented guides, and scholarly analyses—ideal for lawyers, pharmacists, and staff at health authorities, health insurance companies, or the pharmaceutical industry. Typical types of works include commentaries on the AMG, handbooks on medical law, studies on current regulatory issues, and journals such as Arzneimittel & Recht.