Procedures and Requirements for On-Site Inspections and Sampling in Drug Registration (Interim)

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Procedures and Requirements for On-Site Inspections and Sampling in Drug Registration (Interim)

Local Title:药品注册现场核查及抽样程序与要求(试行)
Country/Region:Chinese Mainland
Competent Authority: Former China Food and Drug Administration (CFDA)
Type:Regulation
Status:In force
Release Date:2005-07-19
Implementation Date:2005-07-19

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Document

Language	Source	Title	Access
ZH	Official	药品注册现场核查及抽样程序与要求(试行)	Download

Summary

The Procedures and Requirements for On-site Inspections and Sampling in Drug Registration (Interim) was issued on Jul.19, 2005.

It is formulated to standardize the on-site verification and sampling behavior of drug registration inspection, verify the authenticity of drug registration declaration data.