FDA发布定稿指南，明确特定生物制品CMC上市后生产变更在年报中的记录要求
CMC Postapproval Manufacturing Changes for Specified Biological Products To Be Documented in Annual Reports
FDA发布编号FDA-2017-D-2802的定稿指南，为特定生物制品BLA持有人说明哪些CMC上市后生产变更可记录于年报。指南描述FDA通常认为对产品质量产生不利影响可能性极小的CMC上市后变更。按21 CFR 601.12，此类变更须由申请人在年报中记录，指南意见可随时按21 CFR 10.115(g)(5)提交。
该定稿指南列出特定生物制品BLA持有人可记录于年报的CMC上市后变更类型，便于核对21 CFR 601.12下的记录范围。
GUIDANCE DOCUMENT
Final
- Docket Number:
- FDA-2017-D-2802
- Issued by:
-
Guidance Issuing Office
Center for Biologics Evaluation and Research
Center for Drug Evaluation and Research
This guidance provides recommendations to holders of biologics license applications (BLAs) for specified biological products regarding the types of changes to an approved BLA to be documented in an annual report under 21 CFR 601.12. Specifically, the guidance describes chemistry, manufacturing, and controls (CMC) postapproval manufacturing changes that FDA generally considers to have a minimal potential to have an adverse effect on product quality. Under FDA regulations, postapproval changes in the product, production process, quality controls, equipment, facilities, or responsible personnel that have a minimal potential to have an adverse effect on product quality must be documented by applicants in an annual report.
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-2017-D-2802.
来源：FDA Pharmaceutical Quality Documents · fda.gov