Content Uniformity

Uniformity of Content and Assay is a pharmaceutical analysis technique for the quality control of hard shell gelatin capsules or tablets. The test for Content Uniformity is required for Coated Tablets, Transdermal systems, Suspensions, Inhalations, Solids and Suppositories etc.

It is performed using 10 or 20 Tablets. The solid dosage are dissolved in a solvent then filtered. The filtrate is loaded onto our ASP2000 Workstation where the samples can be further diluted, treated and measured on UV or HPLC. Can be used for UV or HPLC Chromatography Data System detection.



  • Different Dilution ratios, infinitely variable from 1 in 25 to over 1 in 1000
  • Reagent Addition to Stabilise the API or enhance sample detection
  • Up to 240 positions for Samples, Blank and Standards
  • Preparation of Multiple Standards from a stock solution for System Suitability and Standard Checks with Bracketing and Calculation Standard configuration
  • Calculations for Multicomponent Analysis using Fixed Wavelengths or Spectral Scanning and Derivatives
  • Display of results Numerically or in Bar Graph format

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