USP, through the International Training Program (ITP), provides an open forum of discussion in which our processes and approaches to developing public quality standards can be shared with regulatory agencies and reference laboratories around the world. As part of this year’s program we hosted – among others – scientific experts from the Russian Federation.
Validation and verification of analytical procedures are quality assurance activities with broad impact in laboratory operations. Learn USP's role in the development of guidelines in these areas and how to contribute to the discussion.
Access to quality care and medicines is an integral part of public health. For USP, an organization that creates and promotes public standards for medicines and foods, quality and access are two sides of the same coin and in fact the absence of either one actually threatens effectiveness of medical care around the world.
Like most African countries, the challenges facing the Zambian pharmaceutical industry are vast. But under the leadership of Ms. Esnart Mwape, Director General of the Zambia Medicines Regulatory Authority, challenges such as counterfeit drugs are being addressed, as the Authority respositions itself to take charge of the market. Read more.
In Liberia, sellers of poor-quality medicines are capitalizing on public fears about Ebola. Learn what the Liberia Medicines and Health Products Regulatory Authority is doing about it and how the Promoting the Quality of Medicines Program--a collaborative effort between USAID and USP--is playing a role.
While USP is most well-known for its quality standards for medicines and their ingredients, USP also has initiatives focused on food ingredients, dietary supplements and other areas associated with the global supply of medicines. In celebration of World Quality Month, read more about USP's efforts related to product quality and standards.