FDA (Food and Drug Administration) ' s Role in Medical Device Cybersecurity: Dispelling Myths and Understanding Facts

U.S. Food and Drug Administration. 02/17/2017 This one-page fact sheet discusses the Food and Drug Administration ' s premarket and postmarket guidances that offer recommendations for comprehensive management of medical device cybersecurity risks and continuous improvement throughout the total product life-cycle, and incentivize changing marketed and distributed medical devices to reduce risk. A table details Dispelling the Myths, and Understanding the Facts. (PDF)

https://disasterlit.nlm.nih.gov/record/14905

Source: Disaster Lit: Resource Guide for Disaster Medicine and Public Health - May 16, 2017 Category: International Medicine & Public Health Authors: The U.S. National Library of Medicine Source Type: news

More News: Databases & Libraries | Food and Drug Administration (FDA) | International Medicine & Public Health | Medical Devices