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Triclinic Labs is a global leader in solid-state materials characterization and development with more than three decades of trusted experience. We offer comprehensive solid form screening and development services (polymorph, salt, cocrystal, non-crystalline/amorphous materials, formulation, crystallization method development) including intellectual property support for patent claim construction. Our labs are registered and inspected by the FDA to enable cGMP solid mixture method development, validation, and lot release of drug substance and drug product. Our DEA Schedule I-V registration allows us to handle virtually any pharmaceutical material not requiring full containment. We provide comprehensive cGMP and non-GMP routine analytical services for pharmaceutical and specialty chemical manufacturers including XRD, NMR (solids and liquids), IR, FTIR, Raman (dispersive, low frequency, FT), Optical, Digital, Hotstage, and SEM microscopy, DSC, TGA, DVS, HPLC, GC, ICP-MS, KF, and contaminant and counterfeit identification. Visit us during the show at booth 255 to discuss your development needs and challenges or visit https://tricliniclabs.com for more info.