Ryan Panchadsaram, Jess Jacobs, and Stanley Crane respond to questions on m-Health, device regulation, FDA expansion, and patient safety in this question and answer segment.
Stanley Crane, Chief Innovation Officer at Allscripts, speaks to the expanding possibility for creativity for designers and new startups. He strives to harness the latest software development, QA, database, Web and infrastructure technologies to solve business problems and fundamentally change the … Continued
Jess Jacobs from the FDA talks about the realities of how the FDA and the market work together, and what FDA device regulations means for developers, designers, and entrepreneurs.
Matthew Holt covers Medicare, Medicaid and how the Affordable Care Act is changing the status quo in today’s health care system.
White House Fellow Ryan Panchadsaram dives into the mechanics of the Federal Government’s extraordinary activities to stimulate IT in health.
Speakers: Ryan Panchadsaram
Jeff Schox, Scott Jenkins, Deven McGraw, Kim Tyrrell-Knott, and Scott Edelstein respond to questions regarding the legal relationship between health technology companies and patient protection/ HIPA compliance.
Understand what investors expect of your digital IP protection in Jeff Schox’s talk “When You Should Worry about Digital Health Patents.”
FDA expert, Kim Tyrrell-Knott shares her insight on FDA regulation of medical devices, FDA definitions of a product or lack thereof, and what government oversight could mean for a digital health ecosystem.
Scott Edelstein covers legal concerns with telemedicine and mobile health and offers his tips for navigating critical legal issues in developing health apps for remote diagnosis, monitoring, or treatment.
Deven McGraw utilizes her legal background and experience to explain privacy policies, security issues and exceptions, and HIPA compliance for health technology companies.