Finished Product Testing Services
Following is a list of USP tests that we manage for finished non-complex active drug products of our clients. Apart from that we also manage the tests against the non-compendial test method/specifications that may include the in-house, professed, regulatory agency's approved or customized.
DESCRIPTION
- Nomenclature
IDENTIFICATION
- Identification Tests- General
- Spectrophotometric Identification Tests
- Thin-Layer Chromatographic Identification Tests
- Salts of Organic Nitrogenous Bases
- Chromatography
- Capillary Electrophoresis
- Mass Spectrometry
- Spectrometry and Light-Scattering
ASSAY
- Antibiotics- Microbial Assays
- Amphetamine Assay
- Antimicrobial Agents-Content
- Assay for Steroids
- Barbiturates Assay
- Epinephrine Assay
- Nitrite Titration
- Salts of Organic Nitrogenous Bases
- Titrimetry
- Alcoholic Determination
- Chromatography
- Capillary Electrophoresis
- Polarography
- Spectrometry and Light-Scattering
- Ion Chromatography
IMPURITIES
Organic Impurities
- Nitrogen Determination
- Ordinary Impurities
- Chromatography
- Capillary Electrophoresis
- Optical Rotation
- Polarography
- Spectrometry and Light-Scattering
- Impurities in Official Articles
Inorganic Impurities
- Residue on Ignition
- Plasma Spectrochemistry
- Loss on Ignition
Residual Solvents
- Chromatography
SPECIFIC TESTS
Water Content
- Titrimetry
- Loss on Drying
- Thermal Analysis
- Water Determination
Performance Tests
Ophthalmic
- Metal Particles in Ophthalmic Ointments
- Ophthalmic Ointments
- Osmolality and Osmolarity
- Particulate Matters in Ophthalmic Solutions
- pH
Parenteral
- Biological Reactivity Tests, In Vitro
- Biological Reactivity Tests, In Vivo
- Elastomeric Enclosures for Injectables
- Globule Size Distribution in Lipid Injectable Emulsions
- Particulate Matter in Injections
- pH
Oral
- Acid-Neutralizing Capacity
- Disintegration
- Dissolution
- Drug Release
- Uniformity of Dosage Units
- Acoustic Emission
- Intrinsic Dissolution
- In Vitro and In Vivo Evaluation of Dosage Form
- In Vivo Bioequivalence Guidances
- The Dissolution Procedure: Development and Validation
- Tablet Friability
- Tablet Breaking Force
- Oral (Oropharyngeal)-
Topical
- Drug release
- pH
Inhalational
- pH