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0019.860039
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006m     o  d f      
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008180802t20192019onc     o    f000 0 eng d
020 |a9780660274706
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH13-9/24-2019E-PDF
24500|aGuidance document : |bquestions and answers : plain language labelling regulations for prescription drugs.
24630|aQuestions and answers : |bplain language labelling regulations for prescription drugs
24617|aPlain language labelling regulations for prescription drugs
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |c2019.
264 4|c©2019
300 |a1 online resource (34 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline ressource|bcr|2rdacarrier
500 |aIssued also in French under title: Ligne directrice : questions‐réponses : le règlement sur l'étiquetage en langage clair pour les médicaments sur ordonnance.
500 |aCover title.
500 |a"Date adopted: 2015/04/30. Effective date: 2019/08/08. Revised date: 2019/08/08."
500 |a"Publication date: August 2019."
500 |a"Pub.: 180206."
500 |aIssued also in PDF format.
520 |a"This document provides information for industry on how Health Canada’s Health Products and Food Branch interprets and applies the 2014 Regulations Amending the Food and Drug Regulations (Labelling, Packaging and Brand Names of Drugs for Human Use) for prescription products and those administered or obtained through a health professional. Please note that this includes prescription pharmaceutical drugs, biologic drugs (Schedule D), and radiopharmaceuticals (Schedule C). This document does not address implementation for non-prescription products, which are addressed under the Guidance Document: Questions and Answers: Plain Language Labelling Regulations for Non‐prescription Drugs"--Overview, page 8.
69207|2gccst|aPrescription drugs
69207|2gccst|aDrug labelling
7101 |aCanada. |bHealth Canada.
77508|tLigne directrice : |w(CaOODSP)9.860040
85640|qPDF|s690 KB|uhttps://publications.gc.ca/collections/collection_2019/sc-hc/H13-9-24-2019-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/questions-answers-plain-language-labelling-2019/document.html