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USP Convention Meeting 2025

As we enter the new 2025-2030 cycle, we recognize progress made, reflect on the lessons learned, and celebrate the impact we have created on patient and consumer safety.

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Newsroom

Read our latest statements and press releases.

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History of USP

USP has been building trust in medicine for over 200 years.

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Newly elected Council of Experts

The governing body guides USP’s development of quality standards for medicines, dietary supplements, and food ingredients.

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Recognition of Monograph and Reference Standard Donors

The companies listed are those who donated in the last calendar year.

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Comment on Current Proposals in the Pharmacopeial Forum

Your comments on USP’s proposed public standards play a key role in USP’s standards-setting process by helping to shape the content of new and revised standards.

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Global health projects

Our global health projects work to bolster health systems, build medicine supply chain resilience, and improve health equity.

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APEC Supply Chain Security Toolkit

The Toolkit is a resource that addresses areas of vulnerability in the medical product supply chain through prevention, detection, and response strategies and actions.

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Complex Generics

Addressing barriers to the development of complex generics: Understanding challenges and opportunities.

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Atypical Antipsychotics

Validated methods and highly-characterized reference standards are critical for accurate and reliable analytical results.

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Gene Therapy Analytical Guide

Explore the new Gene Therapy Analytical Guide, an online interactive tool that places quality control solutions at your fingertips.

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Extractables and Leachables

E&Ls can adversely impact a drug's potency, stability, safety, and/or effectiveness, which makes their analysis critical.

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Unvalidated methods for medicine quality testing lead to misleading results

The use of unvalidated methods can lead to incorrect results, misinformation about medicine quality and a range of other harmful consequences.

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Powerful qNMR analysis made easy

USP-ID, delivered by Mestrelab Research, is a one-click, automated software solution for identifying, quantifying and labelling a broad range of chemical components in both simple solutions and complex mixtures by qNMR.

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Pharmaceutical Continuous Manufacturing (PCM)

One way that USP assists manufacturers who are considering adoption of PCM is with technical guides that can help them ensure quality.

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Expert Committee/Panel Meeting

Pharmaceutical Analysis Lifecycle & Data Science Expert Committee Official Meeting

January 14, 2026 | January 14, 2026

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