April 24, 2024, 8:10 p.m. |

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Medical device makers submitting products for premarket approval by the Food and Drug Administration often struggle the most with cybersecurity in three major areas - design controls, providing a software bill of materials and testing, according to Nastassia Tamari of the FDA.

administration bill controls cybersecurity design device drug fda focus food food and drug administration major makers materials medical medical device premarket products software software bill of materials testing

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