16 Dec, 2024 NIS2 Series, Part 3 - What happens if you don’t comply? An overview of enforcement, supervisory measures, and liability for management bodies By Andreas Rüdiger Philipp Adelberg Introduction The NIS2 Directive (NIS2 or the Directive) introduces extensive new cybersecurity requirements for a wide range of...
25 Oct, 2023 Artificial Intelligence and healthcare: the Italian DPA adopts a decalogue on GDPR compliance of national healthcare services using AI By Cristina Criscuoli The use of artificial intelligence (‘AI’) systems in the pharmaceutical and healthcare sectors is growing exponentially, with...
18 Oct, 2023 Announcing AI ChatRoom – conversational videos about the rapidly evolving legal landscape of AI - Episode 1: AI + Compliance + Litigation By Danny Tobey DLA Piper is pleased to present AI ChatRoom, a captivating series of conversational videos created to help businesses understand the...
16 May, 2023 The future of the assisted reproductive technology (ART): Modernising ART processes with AI By Nicholas Tyacke Greg Bodulovic Alexandra de Zwart Abi Ketheeswaran +1 more... Show less Assisted fertilisation processes involve striking the perfect balance between a range of complex factors – all of which play a critical...
03 Apr, 2023 New Guidance from the Medicines & Healthcare products Regulatory Agency (MHRA) on the Intended Purpose Statement for Medical Device Software By Poppy Williams As part of the MHRA’s Software and AI as a Medical Device Change Programme, the MHRA has recently published guidance on crafting an...
14 Mar, 2022 Breaking taboos: the ascension of FemTechs in the healthcare market By Bruna Rocha Victoria Cristofaro International Women's Day, celebrated every March 8, focuses on the achievements of women over the years in the cultural, political and...
07 Mar, 2022 HealthTech - Shifting Landscapes Series (Part 1): Overview By Hannah Gardiner HealthTech: Trends and Challenges In a recent internal webinar, DLA Piper and Global Data looked into the shifting landscape of...
21 Sep, 2021 Open consultation on the future regulation of medical devices in the United Kingdom By Richard Taylor Elinor Cavil Background The Medicines & Healthcare products Regulatory Agency (MHRA) is holding an open consultation to gather views on possible...
02 Mar, 2021 Telehealth - a white hot M&A market? By Moritz von Hesberg The global outlook for M&A in the digital health and particularly the telehealth sector has never been brighter than today. Telehealth’s...
22 Feb, 2021 EUDAMED: streamlining the registration process between Legacy and Regulation Devices By Kate Black The European Commission has published a guidance document aiming to further assist manufacturers with understanding how Legacy Devices...
08 Dec, 2017 FDA and the Future of Digital Health By Becca McKnight New guidance just out from FDA on its approach to the regulation of digital health. For companies pursuing opportunities where...
10 Nov, 2017 Medical devices and the smartphone's growing influence By DLA Piper Like many, I love finding out about how technology is shaping our lives and changing society. Deloitte's new research on smartphones...