Medtech

In Europe the European medical device regulation (MDR) is having a significant impact on how medtech manufacturers operate, and in addition there are certain global trends that require medtech manufacturers to reassess, among other things, the way they deliver value to the healthcare ecosystem. At Cirio we advise early stage medtech companies as well as global medtech organizations across the sector including digital health. Cirio’s medtech team acts as legal and strategic partner in matters facing medtech organizations, such as R&D projects, IP protection, commercialization matters, regulatory and compliance matters, global sales and distribution arrangements, public procurement, and legal issues surrounding digitalization and data. Cirio is also uniquely qualified to assist in transactional matters involving medtech such as seed/venture capital financing, M&A, partnering/licensing arrangements, IPO’s, and public take overs.