StartUPDATES: New developments from healthcare startups
Read new developments on healthcare startups such as Seven Bridges, Scipher Medicine, Applied VR and more.
What’s the regulatory framework for neuroprosthetic devices?
Companies developing deep brain stimulation and other neurostimulator technologies that can control and communicate signals to and from artificial body parts (i.e. limbs, eyeballs) are the latest players in the medical device sector.
With the Rise of AI, What IP Disputes in Healthcare Are Likely to Emerge?
Munck Wilson Mandala Partner Greg Howison shared his perspective on some of the legal ramifications around AI, IP, connected devices and the data they generate, in response to emailed questions.
What do you need to know to comply with Phase 3 of FDA’s Unique Device Identification System?
With less than 4 months for the implementation of the FDA’s third phase of the UDI system, companies with Class II devices need to ensure steps are taken to establish UDI for their products.
Health IT biz develops regulatory compliance hub for life science companies, but can it compete with CROs?
Health IT company RegDesk developed a network of regulatory compliance consultants across 140 countries to help life science companies navigate the path to market. Now it’s preparing to roll out a new product that would automate the process of renewing licenses for companies’ products in these countries. In a phone interview with MedCity News, the […]