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  • US Pharmacopeia (USP)
    Featured Solutions Learn about USP’s portfolio of solutions to help address quality assurance, enhance regulatory predictability, and help manufacturers distribute quality medicines, dietary supplements and foods
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    Important Note : Due to ongoing conflict in the Middle East, transportation routes and air capacity across the region are currently disrupted As a result, shipments from the United States to some Middle Eastern destinations and other destinations may experience delays or temporary service suspensions Please note that certain commodities—including dangerous goods, dry ice, and other
  • USP Authorized Distributors
    USP has authorized distribution by the entities listed on this page
  • CERTIFICATE OF ACCREDITATION - US Pharmacopeia (USP)
    CERTIFICATE OF ACCREDITATION The ANSI National Accreditation Board Hereby attests that US Pharmacopeia-India (P) Ltd Plot D6 D8, IKP Knowledge Park, Genome Valley Shamirpet, Turkapally Village Medchal (Malkajgiri) District, Hyderabad 500 101 Telangana, India Fulfills the requirements of ISO IEC 17025:2017 In the field of
  • [Estriol (100 mg)] - CAS [50-27-1] - USP
    View the USP Certificate or Product Information Sheet in the table above to view additional product details, including available label text and storage information 1 The Harmonized System (HS) code provided on this webpage is for informational purposes only and is subject to change without notice
  • CERTIFICATE OF ACCREDITATION - US Pharmacopeia (USP)
    This is to certify that US Pharmacopeia-India (P) Ltd Plot no D6 D8, IKP Knowledge Park, Genome Valley Shamirpet, Turkapally Village Medchal District, Hyderabad 500 101 Telangana, India has been assessed by ANAB and meets the requirements of international standard ISO IEC 17025:2005 while demonstrating technical competence in the field of
  • Dissolution Performance Verification Testing (PVT) | USP
    The USP Performance Verification Test (PVT) is an integral part of the General Chapter 711> Dissolution and assesses proper dissolution apparatus performance
  • Polyethylene Glycol - USP
    Although the Polyethylene Glycol monograph is under the Pharmacopeial Discussion Group (PDG) for harmonization among European Pharmacopeia, Japanese Pharmacopeia, USP, and recently India Pharmacopeia, it has not reached to the harmonization consensus yet, so the above revisions are for the USP Polyethylene Glycol monograph only
  • Pharmaceutical Analytical Impurities - go. usp. org
    USP’s Pharmaceutical Analytical Impurities, like official USP Reference Standards, can help you to save time and resources, and reduce risks associated with quality and consistency related to nitrosamine drug substance-related impurities (NDSRIs) Already know what you need? Go directly to our online store





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