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