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NSF Pharmalytica - 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).
NSF Pharmalytica


NSF Pharmalytica Summary Description:
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).


CONTACT
719 Middle Street
Bristol,CT,06010
US
 
Phone:
Fax:
Email:
NSF Pharmalytica Media Agent
TECHNICAL INFORMATION

NSF Pharmalytica Testing, Assays, Research and Development Services List :

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



 
NSF Pharmalytica Certifications, Accreditations, Licenses:

**Important Note This information has been provided by the Company and has not been confirmed by Contract Laboratory Inc. It is recommended that you confirm all information prior to using this Company .
US Food and Drug Administration Good Laboratory Practices FDA GLP, US Food and Drug Administration Good Manufacturing practices, FDA GMP, DEA licensed for Controlled Substances(Schedule I-V)



 
NSF Pharmalytica Methodologies:

US Food and Drug Administration Good Laboratory Practices FDA GLP, US Food and Drug Administration Good Manufacturing practices, FDA GMP, USP, EP, BP and JP




FEATURED

Lab Services and Lab Products

 

NSF Pharmalytica - 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

Our decades of method development and validation experience are ready to take on your challenging project!

 
NSF Pharmalytica - 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
NSF Pharmalytica conducts a wide variety of compendial tests from USP, EP, BP and JP for both API and excipients.>>


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