美国FDA 指导原则 SPL技术质量体系标识内容标准 英文原版.pdfVIP

Guidance for Industry SPL Standard for Content of Labeling Technical Qs As DRAFT GUIDANCE This Guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance.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, Rockville, MD 20852. All comments should be identif