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美国FDA分析方法验证指南中英文对照
I. INTRODUCTION
This guidance provides recommendations to applicants on
submitting analytical procedures, validation data, and samples to
support the documentation of the identity, strength, quality,
purity,
and potency of drug substances and drug products.
1. 绪论
本指南旨在为申请者提供建议,以帮助其提交分析方法,方法验证资料和样品用于支持原料药和制剂的认定,剂量,质量,纯度和效力方面的文件。
This guidance is intended to assist applicants in assembling
information, submitting samples, and presenting data to support
analytical methodologies. The recommendations apply to drug
substances and drug products covered in new drug applications (NDAs),
abbreviated new drug applications (ANDAs), biologics license
applications (BLAs), product license applications (PLAs),
and supplements to these applications.
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