ComplianceOnline

FDA Guidance on Postmarket Management of Cybersecurity in Medical Devices

  • By: Staff Editor
  • Date: February 16, 2017
  • Source: http://www.fda.gov/
Abstract:

FDA Guidance on Postmarket Management of Cybersecurity in Medical Devices

The significant technological advancements in medical device in today’s world has laterally increased the risk of cybersecurity breaches that could affect device’s performance and functionality. Hence, medical device manufacturers are required to consider cybersecurity throughout the product lifecycle, including during the research and development, design, production, distribution, and maintenance of the device.

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