How can quality standards help reduce the environmental impact of pharmaceutical manufacturing?

New boxes for USP reference standards boost recyclability, cut waste

Explore USP's portfolio mAb solutions

Thank You, USP Expert Volunteers!

Reducing environmental impact of pharmaceutical manufacturing with USP public quality standards

Fireside chat on regulatory convergence with Honorable Dr. Oh Yu-Kyoung, Republic of Korea

Accelerate generic drug development and time to market

Good Manufacturing Practices (GMP) Assessment in Burma

Webinar - New Resources for Adopting, Implementing, and Managing Facilitated Regulatory Pathways

Webinar: Promoting Medical Product Quality Assurance to Achieve Better Health Outcomes

Explore USP’s state-of-the-art Facilities

USP Heroine of Washington | Debbie Miller

USP Verification Programs Overview

Verifying pharmaceutical quality: Standards

Standards mean medicines you can trust

Mitigating Cancer Drug Shortages Event with ACS, ACS CAN & USP Convention

PQM+ NTD Dashboard Launch

Overview and Tutorial of the Updated USP-NF/PF Online Application

Applying Filters to Improve Search Accuracy in USP-NF/PF (Recorded Webinar)

Tackling nitrosamine impurities in medicines

Protecting patients from poor-quality medical products in Cambodia and Laos

Securing the downstream supply chain: post-marketing surveillance

Safeguarding patients from impurities in the drug supply chain

Securing the downstream supply chain: good distribution practices

Experiences Strengthening Quality Assurance in APEC region

Manufacturing Solutions to strengthen global supply chain resilience

The U.S. Capital Region’s Role in Enabling Global Medicines Supply Chain Resilience

Identifying vulnerabilities in the upstream supply chain

Mitigating and managing risks in excipient quality

Pharmacopeial Alert 49(2) - Glass Containers 660 & Selective Drug Product Monographs