Catalin Cimpanu, writing for BleepingComputer: The US Food & Drug Administration plans to ask Congress for more funding and regulatory powers to improve its approach towards medical device safety, including on the cybersecurity front. An FDA document released this week reveals several of the FDA’s plans, including the desire to force device makers to include mandatory update systems inside products for the purpose of delivering critical security patches.
In addition, the FDA also plans to force device makers to create a document called “Software Bill of Materials” that will be provided for each medical device and will include software-related details for each product. Hospitals, healthcare units, contractors, or users will be able to consult the medical device’s bill of materials and determine how it functions, what software is needed for what feature, and what technologies are used in each device.
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