Drug Formulation, Stabilisation & Delivery Services to suit your pharmaceutical development needs
Stability, Bioactivity & Release
Accelerated stability studies provide first insight of efficient formulation composition and process and help in the selection of Lead Candidate.
Testing for impurities, aggregation and degradation products is performed by DSC, DLS, UV spectroscopy, HPLC or as necessary.
Customised drug release studies are designed and performed when required.
ELISA-based and cellular in vitro biological activity assays provide information on stability and preservation of bioactivity.
Formal (GLP) stability studies and animal studies are subcontracted and provide support to regulatory dossiers and drug master files.