The US Food and Drug Administration has published draft guidance updating its definition of a device in accordance with the 2021 Safeguarding Therapeutics Act. The document – published 10 November – ...
As Kenya moves to implement its controversial Anti-counterfeit Act, which effectively outlaws generic drugs, WTR examines the problem with the term 'counterfeit medicine' and why it troubles brand ...
While the government and the industry thrashed out a semblance of consensus on India's viewpoint on the definition of counterfeit drugs that will be presented at the WHO executive board meeting later ...
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