Inorganic Ventures USP Compliance Standards – Ensuring Pharmaceutical & Laboratory Accuracy
Inorganic Ventures offers a specialized range of USP Compliance Standards, designed to meet the stringent requirements of United States Pharmacopeia (USP) testing protocols. Our high-purity Certified Reference Materials (CRMs) support pharmaceutical, biotechnology, and laboratory applications by ensuring accuracy, consistency, and regulatory compliance in elemental impurity analysis.
Manufactured under ISO 17034 and ISO 17025 guidelines, our USP compliance standards are NIST-traceable, providing laboratories with the confidence needed for USP <232>, <233>, and <2232> compliance. These standards are specifically formulated for use in ICP, ICP-MS, and AA techniques to meet pharmaceutical industry regulations regarding elemental impurities in drug substances, excipients, and finished products.
We offer both single-element and multi-element solutions, carefully prepared in acid matrices that enhance stability and compatibility with a variety of analytical instruments. With strict quality control and rigorous testing, Inorganic Ventures ensures that our USP standards deliver the precision required for pharmaceutical quality control and research applications.
Trust Inorganic Ventures’ USP Compliance Standards to help your laboratory achieve regulatory compliance with the highest level of accuracy and reliability. Our commitment to innovation, quality, and customer support ensures that you receive the best solutions for your analytical needs.
For more information, explore our comprehensive selection of USP compliance standards tailored to meet your specific requirements.
