Posted 09 May 2017
By Mukesh Kumar, RAC, Eliane Barras, MSc, Lewis Lau, RAC
This article provides an overview of global regulatory harmonization initiatives and addresses how various regulatory and other organizations are working toward improving access to medicinal products, such as pharmaceuticals and medical devices, and increasing quality through internationally harmonized inspection standards.
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Categories: Biologics and biotechnology, Drugs, Medical Devices, Compliance, Features, US, Canada, Europe, Asia, Latin America and Caribbean, Africa, Middle East, Oceania, ICH, IMDRF, GHTF, APEC, OECD, WHO, ISO