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008220705t20242024onc     ob   f000 0 eng d
020 |a9780660444086
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH139-43/2024E-PDF
24500|aAnnex 3A to the Good manufacturing practices guide : |bschedule C drugs (GUI-0026).
250 |aVersion 3
264 1|a[Ottawa] : |bHealth Canada = Santé Canada,|c2024.
264 4|c©2024
300 |a1 online resource (22 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aCover title.
500 |aDate issued and implemented: 3 July 2024.
500 |aReplaces: Guidance document Annex 3 to the current edition of the Good manufacturing practices guidelines - schedule C drugs (GUI-0026), 19 November 2010.
500 |aIssued also in French under title: Annexe 3A des Lignes directrices sur les bonnes pratiques de fabrication : drogues de l'annexe C (GUI-0026).
504 |aIncludes bibliographical references (page 22).
520 |a"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.
650 0|aRadiopharmaceuticals|zCanada.
650 0|aDrugs|xLaw and legislation|zCanada.
650 0|aDrug factories|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tAnnexe 3A des Lignes directrices sur les bonnes pratiques de fabrication : |w(CaOODSP)9.913040
85640|qPDF|s378 KB|uhttps://publications.gc.ca/collections/collection_2024/sc-hc/H139-43-2024-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/good-manufacturing-practices/guidance-documents/annex-3-current-edition-guidelines-schedule-drugs-0026.html