美国FDA 指导原则 处方药和医疗器械促销中的风险信息呈现 英文原版.pdfVIP

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美国FDA 指导原则 处方药和医疗器械促销中的风险信息呈现 英文原版.pdf

Guidance for Industry Presenting Risk Information in Prescription Drug and Medical Device Promotion DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be submitted within 90 days of publication in the Federal Register of the notice announcing the availability of the draft guidance. Submit comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockvill

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