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:
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| Department/Agency | Canada. Health Canada, issuing body. |
|---|---|
| Title | Annex 3A to the Good manufacturing practices guide : schedule C drugs (GUI-0026). |
| Publication type | Monograph |
| Language | [English] |
| Other language editions | [French] |
| Format | Electronic |
| 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 |
| Description | 1 online resource (22 pages) |
| ISBN | 9780660444086 |
| Catalogue number |
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| Departmental catalogue number | 240245 |
| Edition | Version 3 |
| Subject terms | Radiopharmaceuticals -- Canada. Drugs -- Law and legislation -- Canada. Drug factories -- Canada. |
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