Medical devices & diagnostics

Medical devices and diagnostics are quickly evolving, integrating innovative tech solutions that use and generate increasing amounts of data. They have to meet complex regulatory and compliance standards and are often subject to competitive tendering. This type of product asks for lawyers who deliver quick, pragmatic and compliant solutions.

Through our team of sector specialists, we are well placed to advise throughout the product lifecycle. We regularly advise medical device and diagnostics companies on their day-to-day business activities, including product development, certification, promotion and marketing (both B2B and B2C) and post-market responsibilities and liabilities. We also assist with licensing and commercial contracts, intellectual property enforcement, competition, anti-corruption and code compliance issues.

Medical technology companies expanding into e-health can rely on our strong technology, regulatory and data protection practices to tackle the full spectrum of legal challenges. Our teams regularly advise on the regulations applicable to digital health technologies, the associated data protection risks, as well as the commercialisation of e-health technologies and the regulatory frameworks for healthcare services.