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INSPECTION PROCEDURE Final

Procedure for Remote Inspection as a Part of Compliance Inspection on Drugs and Regenerative Medical Products

PMDA/CPE Notification No. 325 Pharmaceuticals & Medical Devices Agency
ABSTRACT — EDITORS' SUMMARY

PMDA procedure for conducting remote inspections. Covers cloud folder structure, document submission, and remote access requirements for overseas sponsors.

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METADATA
TypeINSPECTION PROCEDURE
Year2023
VersionFinal
StatusCurrent
FormatPDF
Pages—
Size197 KB
Last reviewedJUL 2023
SOURCE
PDF · CANONICAL LINK https://www.pmda.go.jp/files/000264404.pdf ↗
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