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      <marc:subfield code="a">H14-588/2007E-PDF</marc:subfield>
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      <marc:subfield code="a">Stakeholder consultation on the proposed regulatory framework for blood and blood components : </marc:subfield>
      <marc:subfield code="b">March-November 2007 : consultation report / </marc:subfield>
      <marc:subfield code="c">Policy and Promotion Division, Centre for Policy and Regulatory Affairs, Biologics and Genetic Therapies Directorate.</marc:subfield>
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      <marc:subfield code="a">[Ottawa] : </marc:subfield>
      <marc:subfield code="b">Biologics and Genetic Therapies Directorate, </marc:subfield>
      <marc:subfield code="c">December 2007.</marc:subfield>
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      <marc:subfield code="a">Issued 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.</marc:subfield>
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      <marc:subfield code="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.</marc:subfield>
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      <marc:subfield code="a">Blood banks</marc:subfield>
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      <marc:subfield code="z">Canada.</marc:subfield>
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      <marc:subfield code="a">Blood</marc:subfield>
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      <marc:subfield code="a">Canada. </marc:subfield>
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      <marc:subfield code="e">issuing body.</marc:subfield>
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      <marc:subfield code="a">Canada. </marc:subfield>
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      <marc:subfield code="t">Consultation des intervenants sur le projet de cadre de réglementation du sang et des composants sanguins : </marc:subfield>
      <marc:subfield code="w">(CaOODSP)9.938684</marc:subfield>
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      <marc:subfield code="q">PDF</marc:subfield>
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      <marc:subfield code="u">https://publications.gc.ca/collections/collection_2024/sc-hc/H14-588-2007-eng.pdf</marc:subfield>
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      <marc:subfield code="u">https://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</marc:subfield>
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