The European Medical Device Regulation (MDR) is significantly impacting how MedTech manufacturers operate across the continent. Moreover, global trends require MedTech manufacturers to reassess factors such as the way they deliver value to the healthcare ecosystem. At Cirio we advise early stage MedTech companies as well as global MedTech organisations across the sector, including digital health. Cirio’s MedTech team acts as legal and strategic partner in matters facing MedTech organisations, such as R&D projects, IP protection, commercialisation, regulatory and compliance, global sales and distribution arrangements, public procurement, and the legal implications of digitisation and data. Cirio is also uniquely qualified to assist in transactions involving MedTech, such as seed/venture capital financing, M&A, partnering/licensing arrangements, IPOs, and public takeovers.