Our full-service laboratory provides industry-leading analytical testing for pharmaceutical and chemical companies worldwide.For more than 30 years, our GMP-compliant team has remained dedicated to treating our clients as partners, and building relationships that last. 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.