Solid Form Screening & Selection

Solid Form Selection

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martedì 12 maggio 2015

For the selection of the optimal API, several solid forms may be available from one molecule. We provide an effective comparative programme that will lead to a better orientation and targeted selection of the optimum solid form of a certain pharmaceutical molecule with requested properties.

  • In vitro bioequivalence studies, which are less variable, easier to control, and can predict the in vivo bioequivalence, saving time and cost
  • Study of the dissolution rate profile of various forms
  • Stability evaluation of various forms at different conditions of temperature and humidity
  • Identification of the best physical form for pre-formulation

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