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how the FDA’s newly proposed rule

Discuss (between 400 and 500 words): (1) some similarities between ISO 13485 and the current 21 CFR Part 820 in regards to QS for medical devices, (2) some differences between ISO 13485 and the current 21 CFR Part 820 in regards to QS for medical devices, and (3) how the FDA’s newly proposed rule on February 23, 2022 may benefit public health. The paper should have an introduction including a history of the two and benefits The paper should have a conclusion Citation should be in AMA-style