FDA 发布 Q4B 附件 6 剂量单位均匀度通用章节最终指南
Q4B Annex 6: Uniformity of Dosage Units General Chapter
FDA 发布 Q4B 附件 6 剂量单位均匀度通用章节最终指南，文件编号为 FDA-2009-D-0011。该附件由 Q4B 专家工作组编写，旨在使选定药典文本在 ICH 地区可互换使用，避免企业重复检测。本次修订修改附件第 II.B(2.2) 节，说明三本药典的验收标准已协调一致，指南意见可随时在线或书面提交。
该最终指南说明本次修订仅调整附件 6 第 II.B(2.2) 节，可帮助读者定位三本药典验收标准的协调表述。
GUIDANCE DOCUMENT
Final
- Docket Number:
- FDA-2009-D-0011
- Issued by:
-
Guidance Issuing Office
Center for Biologics Evaluation and Research
Center for Drug Evaluation and Research
This annex is one in a series of guidance documents that describe the evaluations and recommendations by the Q4B Expert Working Group (EWG) of selected pharmacopoeial texts to facilitate their recognition by regulatory authorities for use as interchangeable in the ICH regions. Implementation of the Q4B annexes is intended to avoid redundant testing by industry. For general information on the Q4B process, the reader is referred to the core guidance Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the ICH Regions. This annex revises annex 6 on uniformity of dosage units general chapter that issued on June 16, 2014. This revision changes section II.B (2.2) of this annex to correctly state that the acceptance criteria are harmonized between the three pharmacopoeias.
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来源：FDA Pharmaceutical Quality Documents · fda.gov