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2931. Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff

2932. Compounded drug products that are essentially copies of a commercially available drug product under Section 503A of the Federal Food, Drug, and Cosmetic Act

2935. Association of patient out-of-pocket costs with prescription abandonment and delay in fills of novel oral anticancer agents

2938. Medicine for the public

2940. Sammy's sister