Learn about USP's involvement in the APEC Life Sciences Innovation Forum and how this group is improving access to quality medical products by helping Asian-Pacific economies prevent, detect and respond to spurious, substandard, falsified, falsely-labelled and counterfeit products in their supply chains.
Discover convenient tools and helpful tips related to using USP Reference Standards in your work. USP Reference Standards are intended for quality control use in conducting assays and tests in USP’s documentary standards for drugs, dietary supplements, and foods.
Find out answers to important questions about your medications during a special live Twitter Chat “Medication Safety 101: Usage, Storage, and Disposal” on March 23. Hosted by the Alliance for Aging Research, in partnership with NCPIE, the Acetaminophen Awareness Coalition, the American Association of Poison Control Centers, and the CHPA Educational Foundation, this online discussion aims to answer common patient questions on how to safely choose, take, store, and dispose of OTC medications.
Anthony Lakavage, Senior Vice President, USP Global External Affairs, shares insights on USP–India's 10th Anniversary and how USP is working globally to increase its impact on improving the quality of medicines, dietary supplements and foods worldwide.
Learn about unique career paths in pharmacy. APhA CEO Thomas Menighan discusses his personal journey in pharmacy and provides insight into non-traditional roles for pharmacists highlighted in the new, free webinar series Careers Beyond the Pharmacy Counter.
New USP General Chapter <800> Hazardous Drugs—Handling in Healthcare Settings provides consistent standards for the handling of hazardous drugs in healthcare settings to help minimize exposure to healthcare workers, avoid unintended and repeated exposures, and reduce the potential for adverse consequences.
Plastic packaging systems play an important role in protecting the drugs we use. However, a drug’s packaging must be compatible with the product and not compromise its stability, efficacy or safety. USP’s Desmond Hunt, Ph.D., provides insight into plastic packaging systems for drugs and how USP standards can support quality in this field.
Quality plays an integral role in connecting medical research and manufacturing to healthcare practice and consumers. The growing study of the microbiome and the potential health benefits of probiotics offers a particularly timely and illustrative example. Learn about the quality standards USP has developed for probiotics and how they could be the unifying thread connecting clinical research to academia, industry and patients/consumers.
Learn about and view the new suite of physical and written standards that USP is developing to help biologics manufacturers develop and analyze therapeutic proteins. New general chapters address analytical procedures for monoclonal antibodies, oligosaccharides, and protein determination.