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resource/cD9uGk5AoEq0Sl-Sa5Xhcw==
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FDA
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Office of Information Management
Postmarket Management of Cybersecurity in Medical Devices: Guidance for Industry and Food and Drug Administration Staff
Medical Devices; Medical Device Data Systems; Final Rule
Draft Software Policy
Mobile Medical Applications: Guidance for Industry and Food and Drug Administration Staff
U.S. v. Rx Depot
Content of Premarket Submissions for Management of Cybersecurity in Medical Devices
Medical Devices: FDA Should Expand Its Consideration of Information Security for Certain Types of Devices
FDA Policy for the Regulation of Computer Products
Guidance for Industry: Internet/Social Media Platforms with Character Space Limitations-Presenting Risk and Benefit Information for Prescription Drugs and Medical Devices
Promotion of FDA-Regulated Medical Products Using the Internet and Social Media Tools
Guidance to Industry: Cybersecurity for Networked Medical Devices Containing Off-the-Shelf (OTS) Software
Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices
Information Technology: FDA Has Taken Steps to Address Challenges but Needs a Comprehensive Strategic Plan
Cyber Crimes Investigation Unit
Center for Devices and Radiological Health
Internet/Social Media Platforms: Correcting Independent Third-Party Misinformation About Prescription Drugs and Medical Devices
Promotion of FDA-Regulated Medical Products on the Internet
Office of Information Management and Technology
Internet/Social Media Platform with Character Space Limitations–Presenting Risk and Benefit Information for Prescription Drugs and Medical Devices
Content of Premarket Submissions for Management of Cybersecurity in Medical Devices-Draft Guidance for Industry and Food and Drug Administration Staff
General Wellness: Policy for Low Risk Devices
Regulated medical device