January 10, 2018 1:00 PM - 2:30 PM PST
Available Live or By Webinar
Click this link to RSVP
101 California Street
San Francisco, CA 94111
Medical devices currently dominate the internet of things. Connected devices – wearable fitness trackers, heart rate monitors, pacemakers, and glucometers – are being joined by even smarter devices for data analytics, to track outcomes and to improve patient care. The pace of innovation is dramatic. But, as you know, with innovation comes evolving regulation.
Using a case study of a notional new device, an interdisciplinary team of Venable lawyers from our healthcare, cybersecurity, HIPAA, FDA, IP, and government investigations teams will address various challenges the medical device manufacturer or medical device software developer faces – securing the clearance for the product (and its related apps), addressing cybersecurity in product design, privacy compliance, anti-kickback concerns, and the post-market considerations of recall, reporting, and potential enforcement by the FDA and FTC.
This program is designed for companies and entrepreneurs developing, manufacturing, selling, and marketing medical devices and related apps. We look forward to ‘connecting’ with you.
W. Andrew (Drew) H. Gantt, III
– Co-chair of Venable's Healthcare Practice Group
Panelists:Thora A. Johnson
– Co-chair of Venable's Healthcare Practice GroupTodd A. Halpern
– FDA ComplianceMichelle C. Jackson
– FDA ComplianceMichael S. Blume
– FDA and DOJ EnforcementAlper T. Ertas
– Intellectual PropertyJami Mills Vibbert
– Privacy and Data Security