Critical Role Of Labelling Management In Regulatory Affairs

Posted by

Andy Thornley
PhD, Senior Regulatory Consultant

Overview

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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