You need your data rapidly to make crucial dosing decisions during a study. We understand that. At Quotient, data are available in the study eCRF within hours of collection ready for remote sponsor access. Built into our processes are services to facilitate real-time data review and interpretation, including:
Study eCRFs are built by our expert programmers using one of the industry standard electronic data capture tools, InFormTM. We understand changes to study designs and dosing are frequent and so our study strategy for study eCRF design is built to be flexible and rapid in implementation of eCRF updates.
Our Data Managers closely scrutinise data and understand how to reach interim and final locks on time. We maintain licencing and electronic versions of industry standard coding systems, such as MedDRA and WHO Drug Reference List.