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Annex 3A to the Good manufacturing practices guide : schedule C drugs (GUI-0026).H139-43/2024E-PDF

"This document is for people who work with Schedule C drugs (radiopharmaceuticals) as: fabricators, packagers, labellers, testers, distributors, importers. The annex will help you understand and comply with Part C, Division 2 of the Food and Drug Regulations"--Purpose, page 5.

Permanent link to this Catalogue record:
publications.gc.ca/pub?id=9.913037&sl=0

Publication information
Department/Agency
  • Canada. Health Canada, issuing body.
TitleAnnex 3A to the Good manufacturing practices guide : schedule C drugs (GUI-0026).
Publication typeMonograph
Language[English]
Other language editions[French]
FormatDigital text
Electronic document
Note(s)
  • Cover title.
  • Date issued and implemented: 3 July 2024.
  • Replaces: Guidance document Annex 3 to the current edition of the Good manufacturing practices guidelines - schedule C drugs (GUI-0026), 19 November 2010.
  • Issued also in French under title: Annexe 3A des Lignes directrices sur les bonnes pratiques de fabrication : drogues de l'annexe C (GUI-0026).
  • Includes bibliographical references (page 22).
Publishing information
  • [Ottawa] : Health Canada = Santé Canada,2024.
  • ©2024
Description1 online resource (22 pages)
ISBN9780660444086
Catalogue number
  • H139-43/2024E-PDF
Departmental catalogue number240245
Edition
  • Version 3
Subject terms
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