FDA是否要求对每年生产的至少一批产品进行长期留样稳定性考察,并向其递交稳定性数据
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FDA是否要求对每年生产的至少一批产品进行长期留样稳定性考察,并向其递交稳定性数据

2023-08-28 16:25 灯下夜读     
逆葬 2023-09-05 17:55

持续稳定性研究,批准后每年至少一批。但是如果还没被官方批准的话?持续稳定性需要做吗?

1个回答

参照FDA Guidance for Industry ANDAs: Stability Testing of Drug Substances and Products, Questions and Answers 原料药和制剂稳定性试验 问题与解答

答案是肯定的。

Q7 Are there changes to postapproval protocols and commitments when ICH stability guidances are implemented because of scale or type of batches submitted?
A7: ICH Q1A(R2), section II, B, 8, Stability Commitment (2.2.8) addresses this question. Section 2.1.8 provides information regarding stability commitment for drug substances.
Also, ANDAs and DMFs should include a commitment to place one batch of drug product and drug substance, respectively, into the annual long-term stability program, and to provide stability data in the annual reports.

识林链接: http://lib.shilinx.com/wiki/index.php?title=ANDAs%3A_Stability_Testing_of_Drug_Substances_and_Products%2C_Questions_and_Answers 

2023-08-29 11:51 Cora     
逆葬 2023-09-05 17:59

批准后每年至少一批持续稳定性研究,那如果三批工艺验证批递交官方后,还没有被官方批准,那每年也需要做持续稳定性研究吗?每年一批的持续稳定性研究是不是批准后开始做的?