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// June 22, 2022
Avoid product recalls - Know your impurities
Impurities are any components that are not active ingredients or excipients, and that can compromise quality in a drug substance or product. Pharmaceutical impurities can be classified as organic or inorganic and include residual solvents. The presence of impurities results from manufacturing and degradation processes.
// June 09, 2022
Pharmaceutical continuous manufacturing: What drug makers need to know...
Pharmaceutical continuous manufacturing (PCM) technology has gained increased attention from industry and policymakers as one way to help expand domestic manufacturing of essential medicines
// June 07, 2022
Volunteer Spotlight: USP Beal Award winner shares perspective on making a difference ...
This spring, long-time USP volunteer Dennis Gorecki, Ph.D., became the latest recipient of USP’s signature Beal Award for outstanding contributions to public health while serving as a USP volunteer.
// May 24, 2022
Supply chain vulnerabilities exist for antimicrobial medicines: USP Medicine Supply M...
Antimicrobial resistance (AMR) is one of the top global health threats. USP's latest analysis shows both an increased risk of shortages for some types of antimicrobials and the geographic concentration of facilities with active Drug Master Files (DMFs) for antimicrobials.