Medical Products | Professional literature for training, studies and practice

In the Medical Device Law category, you will find comprehensive professional literature on the legal framework governing medical devices, pharmaceuticals, and digital health applications. The titles cover key topics such as the EU Medical Device Regulation (MDR), the Medical Device Law Implementation Act (MPDG), compliance requirements, liability issues, and the regulation of smart and digital medical devices. Additionally, they address intersections with related legal fields such as pharmaceutical law, social law, and data protection (GDPR).

The publications are aimed at manufacturers, suppliers, operators, lawyers, and healthcare professionals. They include commentaries, practical handbooks, introductions, journals, and analyses of current developments such as the reprocessing of single-use products, pay-for-performance models, or product liability. Typical types of publications include commentaries, guidelines, commemorative volumes, and legal comparisons.