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Microtest Labs Adds Dissolution Testing to its Suite of Analytical and Stability Testing Services
Date:5/26/2009

opment studies
  • For use in routine QC analysis for lot release and to measure lot-to-lot variability
  • For use in stability studies to study the effects of time/temperature/humidity on the dosage form
  • To compare one dosage form to another (different formulations, different processes, analysis of competitor's samples)
  • To estimate release and absorption rates in humans after an in vitro -- in vivo correlation is established

  • Dissolution is a sample preparation technique. Samples still need to be analyzed separately, usually by Microtest's HPLC or UV Spectroscopy testing. Typical samples are oral dosage forms, although it can also be used on topicals and transdermal systems.

    In addition to dissolution testing, Microtest provides a host of analytical assays, including HPLC Assays, GC Analysis, Protein Analysis, FTIR Analysis, and UV/VIS Analysis.

    Microtest's analytical testing processes follow guidelines from all major standards authorities, including the United States Pharmacopeia (USP), the Japanese and European Pharmacopoeias, the U.S. Food and Drug Administration (FDA), the International Organization for Standardization (ISO), and the Association for Advancement of Medical Instrumentation (AAMI)
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