At Quotient Clinical, our innovative approach to the drug development process goes beyond formulation development and clinical testing. Our clinical study support services include regulatory expertise, adaptive clinical protocol design, on-study safety/PK data review, interim statistical analysis, rapid database lock and full service reporting. Built into these services is our scientific expertise, adherence to industry recognised standards (including CDISC and eCTD) and use of industry standard software (including Oracle InForm, Phoenix WinNonlin and SAS). Operational compliance is ensured by our Quality Management System and program of audits.
More details of our support services can be found below: