e-SOCDAT from the Coordinating Centre's perspective
Centralised
e-Clinical solution uniting interconnected components within a single application and database allowing the collection and management of clinical and operational metadata.
Optimal study design
Efficient study design using reliable, pre-validated data items.
Efficient document management
Electronic management and tracking of the Trial Master File documents, site visit contacts, source data verification and on-site visit reports.
Quality
100% regulatory compliant with quality orientated study and data management processes.
Flexibility
Adjustable system enabling targeted customisation.
Data-driven workflow
Data management processes continuously driven by patient and study data status.
Real-time
Study management streamlined by the effective combination and utilisation of real time study information on an ongoing basis.