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Pharmaceutical Residual Solvents

Pharmaceutical Residual Solvents
2Pages

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Analytical Standards for Pharmaceutical Residual Solvents In the pharmaceutical industry, the guidelines set by the International Conference on Harmonization (ICH) and by United States Pharmacopeia (USP) and European Pharmacopeia (EP) mandate that manufacturing solvents have to be regulated due to their toxic and/or environmentally hazardous nature. For this industry, SPEX CertiPrep has created Pharmaceutical Residual Solvent Certified Reference Materials (CRMs) designed exclusively for GC, GC/MS, HPLC, and HPLC/MS analysis. These standards are made from the highest purity starting materials and the highest grade of solvents available to guarantee superior grade standards. The standards then go through a rigorous QC process where a senior chemist approves the standards. This guarantees the standards are accurate and stable at the stated concentrations for all components. In addition, all standards are supplied with a detailed comprehensive Certificate of Analysis. For additional product information, please visit www.spexcertiprep.com/products/USP. SPEX CertiPrep is the industry leader for over 60 years in the CRM marketplace meeting the needs of laboratories worldwide with innovation and research. Accredited by A2LA to ISO/IEC 17025:2005 & ISO Guide 34:2009. Certified by DQS to ISO 9001:2015.

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SPEX CertiPrep? CAN'T FIND THE STANDARDS YOU ARE LOOKING FOR? SPEX CertiPrep can make custom standards to meet your exact needs. Contact us for more information. © 2017 SPEX CertiPrep. All Rights Reserved. US ADDRESS 203 Norcross Avenue • Metuchen, NJ 08840 Tel: 1.800.LAB.SPEX • +1.732.549.7144 • Fax: 732.603.9647 CRMSales@spex.com • www.spexcertiprep.com

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Pharmaceutical Residual Solvents 2Pages

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Pharmaceutical Residual Solvents
2Pages