Critical Role of Labeling Management in Regulatory Affairs

Andy Thornley

PhD, Senior Regulatory Consultant

Labelling for human healthcare products (i.e. medical devices, medicines, cosmetics,
vitamins, and dietary supplements) is a complex, interdisciplinary function that services
the corporate and regulator-approved prescribing information, instructions for use and
pack information for consumers, patients and healthcare professionals, together with
correct advertising and promotion.

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