Abstract
Part V of the Act specifies the types of controls to be imposed over the packaging and labelling of medicines. The controls are intended to enhance the safety of medicinal products by ensuring that they are correctly described, readily identifiable, and bear appropriate warnings and instructions and that false or misleading information is not given with them, (section 85(2)).
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Reference
Pharm J., 1982, i, 107
Pharm J., 1985, i, 366–7
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© 1986 MTP Press Limited
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Harrison, I.H. (1986). The Packaging and Labelling of Medicines. In: The Law on Medicines. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-4141-0_16
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DOI: https://doi.org/10.1007/978-94-009-4141-0_16
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-010-8337-9
Online ISBN: 978-94-009-4141-0
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