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      <marc:subfield code="a">Good label and package practices guide for prescription drugs </marc:subfield>
      <marc:subfield code="h">[electronic resource].</marc:subfield>
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      <marc:subfield code="a">Ottawa : </marc:subfield>
      <marc:subfield code="b">Health Canada, </marc:subfield>
      <marc:subfield code="c">2016.</marc:subfield>
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      <marc:subfield code="a">iii, 71 p.</marc:subfield>
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      <marc:subfield code="a">Issued also in French under title: Guide des bonnes pratiques d’étiquetage et d’emballage pour les médicaments sur ordonnance.</marc:subfield>
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      <marc:subfield code="a">"June 30, 2016."</marc:subfield>
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      <marc:subfield code="a">Includes bibliographical references.</marc:subfield>
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      <marc:subfield code="a">The objective of the Good Label and Package Practices Guide for Prescription Drugs is to provide direction to sponsors, manufacturers and license holders (to be referred to as ‘sponsors’ within this guide) in designing safe and clear labels and packages. It is essential that all labelling and packaging regulatory requirements be met. The recommendations provided in this guide will aid sponsors in the organization of (a) information required by the regulations, and (b) other complementary information important to the proper identification, selection, and use of the product. The information is presented to support the design and development of labels and packages that are clear, effective, and minimize the risk of errors causing harm.</marc:subfield>
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      <marc:subfield code="t">Guide des bonnes pratiques d'étiquetage et d'emballage pour les médicaments sur ordonnance </marc:subfield>
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