Pre-formulation studies

Dissolution testing

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mercoledì 13 aprile 2016

Drug absorption from a solid dosage form after oral administration depends on the release of the drug substance from the drug product, the dissolution or solubilisation of the drug under physiological conditions, and the permeability across the gastrointestinal tract. Because of the critical nature of the first two of these steps, in vitro dissolution may be relevant to the prediction of in vivo performance.

How can we help you?

  • Assess the lot-to-lot quality of a drug product
  • Guide development of new formulations
  • Ensure continuing product quality and performance after certain changes (i.e. the manufacturing process, the site of manufacture, and the scale-up of the manufacturing process)

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