The healthcare sector is characterized by a highly complex and dynamic regulatory environment. Medical device and pharmaceutical regulations impose stringent requirements on the development, approval, marketing, and monitoring of products. At the same time, companies, service providers, and other market participants are under increasing economic and regulatory pressure.
We support you in reliably classifying legal requirements, managing risks, and reliably structuring your activities in the healthcare market. FGvW provides comprehensive advice on medical device law, pharmaceutical law, and all other issues in the healthcare industry.
We advise our clients in medical device and pharmaceutical law throughout the entire product and service cycle, from initial regulatory classification to market access and distribution to ongoing compliance and conflict resolution. Our approach is practical and aimed at reconciling regulatory requirements with economic objectives.
We take an interdisciplinary and market-oriented approach to healthcare law. Our consultants specifically incorporate related areas of law in order to consistently integrate regulatory, competitive, contractual, and liability aspects. This results in legally compliant structures that offer planning security and support operational processes.
Clear advice and reliable decisions are particularly important in a sensitive and highly regulated environment. We support you in confidently managing regulatory requirements, minimizing risks, and securing your position in the healthcare market in the long term.
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Legal Insights
12. May 2026
Updates in Medical Device Law – Update as of May 11, 2026
At the international level, the regulatory landscape for medical devices is constantly evolving. For all stakeholders, this means staying informed about new developments and adapting internal processes in a timely manner. On May 7, 2026, the European Commission, the Council, and the European Parliament agreed on a reform of the AI Regulation. In its press...
Reading time: 1 min
Medical device law, pharmaceutical law, healthcare
3. December 2025
Updates on the Medical Device Regulation – The EU Takes Action (?)
At the international level, the regulatory landscape for medical devices is constantly changing. For all stakeholders, this means staying informed about new developments and adapting internal processes in a timely manner. With this brief “Update on the Medical Device Regulation,” we would like to summarize some important developments at the EU level. Several EUDAMED systems...
Reading time: 7 min
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