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INSPECTION PROCEDURE Trial Implementation

Work Procedures for Drug Registration Inspection (Trial)

CFDI No. 30 of 2021, Attachment 1 National Medical Products Administration
ABSTRACT — EDITORS' SUMMARY

How NMPA conducts drug registration inspections — procedures, time limits, requirements. Covers clinical trial inspections as part of the broader registration inspection framework. Part of the 5-document CFDI No. 30 set alongside the Key Points documents.

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METADATA
TypeINSPECTION PROCEDURE
Year2021
VersionTrial Implementation
StatusCurrent
FormatPDF
Pages
Size
Last reviewedJAN 2022
SOURCE
PDF · CANONICAL LINK https://english.nmpa.gov.cn/pdf/WorkProceduresforDrugRegistrationInspection-CFDA.docx
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