Postmarket Management of Cybersecurity in Medical Devices

U.S. Food and Drug Administration. (2016). Postmarket Management of Cybersecurity in Medical Devices.
This guidance can help manufacturers and healthcare providers manage cybersecurity in medical devices, particularly those that are networked.
Rate:
Favorite:
1
You must Login to add a comment
  • This item doesn't have any comments

Enter your email address to receive important announcements and updates through the ASPR TRACIE Listserv.