FDA 发布 ICH Q12 药品生命周期管理附录最终指南（FDA-2018-D-1609）
Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management
FDA 发布 ICH Q12 药品生命周期管理附录最终版 Level 1 指南，文件编号 FDA-2018-D-1609，由 CDER 与 CBER 发布。文件说明附录 I.A 至 I.F 的示例为示意性模拟示例，仅提示 ICH Q12 指南第 III、IV、V 节所述工具的可能用法，不应作为申报模板或唯一依据。
材料说明 ICH Q12 附录中 I.A 至 I.F 的示例仅为示意，不宜作为申报模板，并提示报告类别可能因地区法规而异。
GUIDANCE DOCUMENT
Final Level 1 Guidance
- Docket Number:
- FDA-2018-D-1609
- Issued by:
-
Guidance Issuing Office
Center for Drug Evaluation and Research
Center for Biologics Evaluation and Research
The examples provided in sections I.A through I.F of the ICH Q12 Annexes are mock examples provided for illustrative purposes. They only suggest how the tools described in sections III, IV, and V of the ICH Q12 guidance could be applied, and should not be used as a template or the sole basis for a regulatory submission. In addition, the reporting categories, as described in section II of the ICH Q12 guidance, may differ across regions depending on regional legislation; the nature of the product; and the Marketing Authorization Holder’s (MAH’s) demonstrated understanding of the product, process, and analytical procedure.
Submit Comments
You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))
If unable to submit comments online, please mail written comments to:
Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852
All written comments should be identified with this document's docket number: FDA-2018-D-1609.
来源：FDA Pharmaceutical Quality Documents · fda.gov