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008230414e20240521onc     ob   f000 0 eng d
020 |a9780660483740
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH139-49/2024E-PDF
24500|aAnnex 1 to the Good manufacturing practices guide : |bmanufacture of sterile drugs (GUI-0119).
250 |aVersion 2.
264 1|a[Ottawa] : |bHealth Canada = Santé Canada,|c21 May, 2024.
264 4|c©2024
300 |a1 online resource (84 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Annexe 1 des Lignes directrices sur les bonnes pratiques de fabrication : fabrication de médicaments stériles (GUI-0119).
500 |a"Replaces: Annex 1 to the Good manufacturing practices guide: Manufacture of sterile drugs (GUI-0119), February 28, 2018."
504 |aIncludes bibliographical references (page 81).
520 |a"This document provides guidance for fabricating and packaging/labelling sterile drugs"--Purpose, page 5.
650 0|aDrug factories|zCanada.
650 0|aDrugs |xSterilization|zCanada.
650 0|aDrugs|xLabeling|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tAnnexe 1 des Lignes directrices sur les bonnes pratiques de fabrication : |w(CaOODSP)9.921682
85640|qPDF|s820 KB|uhttps://publications.gc.ca/collections/collection_2024/sc-hc/H139-49-2024-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/good-manufacturing-practices/guidance-documents/gmp-guidelines-annex-1-manufacture-sterile-drugs-0119.html