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NSF Pharmalytica

719 Middle Street

Bristol, CT 06010 US


NSF Pharmalytica provides accurate, reliable, timely and cost-efficient contract analytical and manufacturing solutions to pharmaceutical and chemical industry clients. Our laboratories operate under full GLP and GMP compliance, are FDA registered and inspected and DEA licensed to handle, store and test Controlled Substances (Schedule I thru V).

Technical Information:

FDA GMP Analytical Services, Method Development and Validation, Stability Storage and Testing, Extractables & Leachables, Oligonucleotide and Aptamer Analysis, Raw Material Testing, Clinical Services,Clinical Trial Services
Pre-Clinical GLP Testing, Test Article Characterization, Formulation Analysis, Bioanalysis, Pre-Clinical Formulation Development, GLP Services, Physical Properties Determinations, Assay and Impurities, Identification by FTIR, Moisture determination, Residual Solvents, Molecular Weight confirmation by MS, Residue on Ignition, Heavy Metals, Post-Study Stability Analysis, Parent and metabolite ID and Quantitation, Degradation Product / Impurity Profiling and Identification, Metabolic Pathway Elucidation, Drug-Drug Interaction Studies, In-Vitro Metabolism Studies, Assay by HPLC, GC or Titration, Organic Volatile Impurities, Identification by FT-IR, UV-Vis or NMR, Optical Rotation, Metals by ICP, Heavy Metals, Loss on Drying, Moisture by Karl Fischer Titration, Thermal Properties by DSC and TGA, Container and Closure Testing

DISCLAIMER: This Laboratory Profile was provided by the company above.