Calling all #dietarysupplement and #dietaryingredient stakeholders! Participate in USP’s standards development process by submitting your comments on proposed dietary ingredient and dietary supplement monographs today: Broccoli Seed Dry Extract Choline Bitartrate Choline Chloride Choline Citrate Guarana Seed Guarana Seed Dry Extract Guarana Seed Powder Pyrroloquinoline Quinone Disodium Red Yeast Dry Extract Red Yeast Rice Powder Comment by September 30, 2026: https://ow.ly/lTNA50Zyr5U
USP Science & Research
Pharmaceutical Manufacturing
20852, Rockville 12,992 followers
Building trust through rigorous science & standards that ensure quality.
About us
Scientific research and the expertise of our staff and volunteers are at the root of our work in advancing public health by ensuring the quality and safety of medicines, dietary supplements, and food ingredients. We are committed to rigorous science to help protect patient safety, build trust in our public quality standards setting, and improving the health of people around the world. We invite scientists, academics, regulatory professionals, healthcare practitioners, thought leaders, and others to follow this page to stay informed on our latest research publications and announcements on opportunities to serve as decision-makers and advisors on USP’s councils, committees, and panels.
- Website
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https://www.usp.org/our-science
External link for USP Science & Research
- Industry
- Pharmaceutical Manufacturing
- Company size
- 1,001-5,000 employees
- Headquarters
- 20852, Rockville
- Founded
- 1820
- Specialties
- nonprofit, standards setting, and medicines quality standards
Updates
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Better patient outcomes begin with transformative therapies. Delivering them at global scale starts with standards trusted worldwide. Navigating regulatory complexity requires clarity from the start. USP equips teams with trusted quality standards that help reduce analytical uncertainty, support submissions, and strengthen compliance. By incorporating USP standards early in development, teams can help strengthen quality, support regulatory preparedness, and navigate global market expectations with greater consistency and clarity. How does your team navigate regulatory complexity? Discover how USP can help your team succeed. Learn more - https://ow.ly/TASg50Zypx8
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Introducing the redesigned USP Store - Easier access to the standards and solutions you trust . The USP Store has been updated to provide an enhanced experience, helping customers and users move from search to solution with greater ease and confidence. New store features include: ✅Intelligent search Any search you make now predicts what you’re looking for as you type, instantly displaying key scientific identifiers and correcting for typos. ✅Consolidated product pages Product pages group essential information to reduce uncertainty and support your decision-making. ✅Role-based dashboards The platform tailors your dashboard experience to your specific role, whether you’re a scientist or a procurement specialist. ✅Cart sharing and Authorized Distributor (AD) quotes You can now share in-progress carts internally for immediate review and checkout or to generate an automated quote request to selected regional ADs. Learn more about the updated USP Store: https://ow.ly/wgyp50ZyqNZ
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The rapid growth of peptide therapeutics, particularly GLP-1 medicines, is creating new opportunities and new quality challenges for developers and manufacturers. Success depends on analytical methods, effective impurity control strategies, and reliable standards that support product quality from development through commercialization. Join USP's webinar, "Quality Considerations and Analytical Tools for Peptide Therapies, Including GLP-1s, Across the Product Lifecycle," to learn how compendial standards, guidance chapters, and reference materials are helping the industry advance peptide therapeutics with confidence. Key topics include: • Lifecycle approaches to peptide quality and regulatory compliance • Analytical tools for impurity profiling and method development • Expanded USP reference materials for semaglutide and liraglutide • Strategies for assessing identity, purity, strength, and performance across peptide modalities Featuring: Manoj Kumar Metta, PhD, EMBA Principal Scientist, Global Biologics, USP Shankar Sellappan, PhD Senior Product Manager, USP 📅 August 25, 2026 | 60 Minutes Register today! https://ow.ly/4YSh50ZwPpZ #GLP1 #Peptides #Biopharmaceuticals #QualityAssurance #RegulatoryScience #PharmaManufacturing #DrugDevelopment #AnalyticalChemistry #USP
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USP Science & Research reposted this
USP is proud to sponsor and exhibit at the 2026 Bioprocessing Summit, bringing together industry leaders, scientists, and innovators to address the evolving challenges of biologics. Visit us at Booth #320 to learn how USP's standards, reference materials, and expert solutions help strengthen quality, accelerate development, and support confidence across the product lifecycle. Throughout the conference, USP experts will share insights on critical topics including mRNA quality frameworks, rapid microbiological methods, lentiviral vector analytics, AAV quality control, and approaches to analytical standardization for emerging therapeutic modalities. For more information on our scientific sessions and to register, click here: https://lnkd.in/ez5twc3V #CHIBioprocessingSummit Cambridge Healthtech Institute Cambridge Innovation Institute
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USP is proud to sponsor and exhibit at the 2026 Bioprocessing Summit, bringing together industry leaders, scientists, and innovators to address the evolving challenges of biologics. Visit us at Booth #320 to learn how USP's standards, reference materials, and expert solutions help strengthen quality, accelerate development, and support confidence across the product lifecycle. Throughout the conference, USP experts will share insights on critical topics including mRNA quality frameworks, rapid microbiological methods, lentiviral vector analytics, AAV quality control, and approaches to analytical standardization for emerging therapeutic modalities. For more information on our scientific sessions and to register, click here: https://lnkd.in/ez5twc3V #CHIBioprocessingSummit Cambridge Healthtech Institute Cambridge Innovation Institute
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Most laboratories today rely on centralized informatics platforms (LIMS, ELN, CDS) that often operate in silos. In this clip from the CSols Podcast, Kyle L., Sr. Product Manager, Digital & Innovation at USP, discusses USP MethodConnect: vendor-neutral core method data designed to flow into the systems labs already use, supporting consistency within organizations and across global partner networks. Learn more about USP MethodConnect: https://bit.ly/4wLUdS4
As pharmaceutical and life science labs modernize, regulatory and compliance standards have to keep pace. But digital transformation doesn't happen at the same speed for every organization. How can quality bodies support labs embracing AI and connected workflows while ensuring those relying on paper or legacy LIMS aren't left in the dark? In this short clip, Kyle L. at US Pharmacopeia shares how they are evolving both physical and documentary standards to improve traceability, strengthen regulatory confidence, and enable the future of science—no matter where a lab is on its digital journey. Watch the full episode here: https://lnkd.in/gycGMt84 #LabAutomation #PharmaTech #DigitalTransformation #USP #LabInformatics #AIinScience #QualityAssurance #LIMS #CSolsPodcast
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In a digital era... what's important? It's not just technology. As digital tools evolve rapidly, it is imperative to have quality, trusted standards evolve as well. This is where collaboration becomes essential. Michael Levy, SVP of USP's Division and Innovation, reveals how evolving quality standards alongside the pharmaceutical industry includes everyone—from quality, industry, laboratory scientists, regulators, and other professionals. Read more about the future of pharmaceutical standards here: https://ow.ly/U8Bq50ZvmRn
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USP Science & Research reposted this
🔬 Working with monoclonal antibodies? Ensuring consistent and reliable quality assessments for mAbs can be increasingly complex. To help address this, USP now offers product-specific solutions for rituximab and bevacizumab designed to support more reliable and comprehensive analytical evaluation. These include: ✅ Reference standards • Support system suitability • Provide independent, product-specific benchmarks ✅ Emerging standards • Methods for assessing key quality attributes • Enable more flexible, science-based analytical approaches Together, these solutions help: ✔ Improve analytical consistency ✔ Facilitate regulatory alignment ✔ Support broader patient access worldwide Learn more about how USP is advancing mAb analysis with product-specific biologics reference standards and flexible, science driven methods: https://lnkd.in/eMbD_3Qj #USP #Biologics #Biosimilars #mAbs #ReferenceStandards
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Analytical confidence starts with reliable measurements. Yet complex spectra, overlapping peaks, and varying analytical approaches can make quantitative results more difficult to reproduce, interpret, and defend. Quantitative NMR (qNMR) offers a powerful framework for improving quantitative accuracy and consistency by providing traceable measurements and supporting reproducible workflows across laboratories. USP's proposed qNMR emerging standards open scientists to early access to methods under evaluation, creating an opportunity to apply, assess, and provide feedback before any potential formal compendial adoption. Because analytical confidence isn't just being developed for the future. It's being tested, refined, and improved today. How are you improving analytical confidence in your lab? Discover qNMR emerging standards here: https://ow.ly/b9jS50ZtN6w