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.
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这{{threadTextType}}正{{isAdminText}}
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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?