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040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH14-588/2007E-PDF
24500|aStakeholder consultation on the proposed regulatory framework for blood and blood components : |bMarch-November 2007 : consultation report / |cPolicy and Promotion Division, Centre for Policy and Regulatory Affairs, Biologics and Genetic Therapies Directorate.
264 1|a[Ottawa] : |bBiologics and Genetic Therapies Directorate, |cDecember 2007.
300 |a1 online resource (42 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Consultation des intervenants sur le projet de cadre de réglementation du sang et des composants sanguins : mars-novembre 2007 : rapport de consultation.
520 |a"Health Canada’s blood regulatory framework under the Food and Drugs Act is being revised as one element of a renewed Canadian blood system. This initiative will address the safety of whole blood and blood components in Canada by developing updated and/or new specific regulatory requirements that reflect current technology and practices by referencing commonly accepted safety standards"--Overview, page 4.
650 0|aBlood banks|xLaw and legislation|zCanada.
650 0|aBlood|xTransfusion|xSafety regulations|zCanada.
7101 |aCanada. |bBiologics and Genetic Therapies Directorate, |eissuing body.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tConsultation des intervenants sur le projet de cadre de réglementation du sang et des composants sanguins : |w(CaOODSP)9.938684
85640|qPDF|s217 KB|uhttps://publications.gc.ca/collections/collection_2024/sc-hc/H14-588-2007-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/biologics-radio-pharmaceuticals-genetic-therapies/stakeholder-consultation-proposed-regulatory-framework-blood-blood-components-march-2007-november-2007-consultation-report.html