Smooth opens a new bioequivalence center in St.Petersburg
Smooth Clinical Trials opens a new bioequivalence center.
To get a generic drug registered it is necessary to submit results of pre-clinical and local clinical trials.
Due to a well-coordinated team, partnership with clinical sites and bioanalytical laboratories, we guarantee quick study performance with high quality of data and documents.
Smooth Clinical Trials partners with a leading clinical research sites.
Approximate timelines of a bioequivalence trial are 3 months from clinical trial approval to study report.