e-SOCDAT™ from the sponsor’s perspective

Reliable

Fully validated, regulatory compliant and independently audited.

Time efficient

Reduces time from study design to study reporting by optimising all project and data management steps.

Cost conscious

Reduces the need for meetings, manpower, time, paper generation and distribution.

All inclusive

Uniting of clinical and operational metadata within one central platform, facilitating communication and decision making processes.

Panoramic study view

Continuous complete overview of clinical and operational metadata and metrics thanks to customisable listings and real time status reports.

Pharmacovigilance

Reporting timelines guaranteed in addition to timely creation of safety reports (e.g. CIOMS, E2B, SAE narratives) and secured web access for study treatment code break.

Data transfer

Flexible and compliant to any standard data format (e.g. CDISC, ODM).