RML is an FDA-inspected, GMP/GLP compliant analytical laboratory performing USP testing as well as method development and validation services to the pharmaceutical, biotech, academic, and chemical industries. We accept both domestic and international requests. Services include: • USP <232/233> and ICH Q3D Elemental Impurities Testing • Metals Analysis by ICP-OES/ICP-MS (trace levels to percent) • Semi-quantitative Elemental Scans • USP <281> Residue on Ignition • Water Content by Karl Fischer • MicroAsh Analysis • USP <467> Residual Solvents • GC/GC-MS Analysis • HPLC Analysis • CHN Analysis • Halogen/Sulfur Analysis by Titration and Ion Chromatography • DSC/TGA/Melting Point • FTIR/NIR • UV-Vis Spectroscopy • Optical and Spectral Rotation • Method Development • Method Validation and Qualification We have the capabilities and expertise to perform many other USP or analytical analyses. Contact us with your specific test method and requirements for more details and a personalized quote.