Overview
Targeted, efficient and solution-oriented
Your Attorney
Matthias Mock was admitted to practice as a German Attorney in 2006. He started his career as a registered foreign lawyer with the international commercial law firm Travers Smith in London in the areas of IT, IP and commercial law before moving into the MedTech industry.
After more than fifteen years in-house in the MedTech, pharma and life sciences industries, culminating as General Counsel of a medium-sized MedTech firm, Mr. Mock decided in 2024 to parlay his deep industry experience in a focused boutique law firm. In February 2025, he founded mock.legal in Fridingen an der Donau near Tuttlingen, the “world capital of medical technology”.
In his free time, Mr. Mock enjoys exploring the beautiful Upper Danube Valley and is engaged in public life in Fridingen.
Experience & Expertise
- Delivering legal expertise to MedTech clients in the Tuttlingen area
- Fast, tailor-made solutions thanks to industry knowledge and experience
- Direct access and communication
- Contracts and contract negotiations in German and in English at native speaker level
- In addition to German and EU law, experience with both US and UK legal systems
- Technical language proficiency in the MedTech, pharma & life sciences context
- External solution with in-house quality and liability advantage
- Avoidance & hedging of legal risks
- In-depth understanding of industry-specific contract forms and regulations
More about my professional career

Industry focus
On-point advice
Consulting for regulated industries – medical devices, pharma & life sciences. mock.legal offers specialized legal advice along the entire product life cycle – from research and development to market launch.
Medical Device Industry
Of the 1,450 medical device companies active in Germany, around 400 of them are located in the Tuttlingen area, the “world capital of medical technology”. Due to the strong regulation of medical devices, targeted legal support is particularly relevant for companies engaged in their production and distribution.
- Consulting along the entire product life cycle
- NDA, research, development and supply contracts
- License and quality assurance agreements
- EU Medical Device Regulation (MDR)
Pharmaceuticals Legal Advice
As head of legal and compliance functions, Mr. Mock has advised pharmaceutical companies comprehensively on products including innovative pharmaceuticals, biosimilar drugs and generics. He has a particular interest in the legal support of projects involving both pharmaceuticals and medical technology, such as drug delivery devices, insulin pumps or contrast media and other innovative imaging or diagnostic technologies.
Life Sciences Legal Advice
Another focus of the firm is the support of life science projects and cooperations between universities, research institutions and companies, in particular licensing and R&D cooperations. In this context, Mr. Mock also advises start-ups and university spin-offs.