An integrated eclinical platform for fast and easy study setup and smart clinical data management for all phase of clinical trials
Electronic Data Captureadmin2021-09-23T10:35:05+00:00
ClinVigilant Data Management tool provides a highly configured platform to create the eCRF from paper CRF or directly using our Institutive eCRF designer tool.
Faster Study Deployment
Reduce time spent on building and managing studies. Be it single centre or multicentre studies, Clinvigilant EDC’s manage sites, CDASH-CDISC form template builder, advanced user management, workflow, Scheduling and rule configuration will streamline your data capture for all your clinical trials. over 90% of studies being deployed within 4 weeks.
Well-timed Database Lock
Friendly data entry forms empower users to enter data rapidly while ensuring accuracy. Reduce database lock delays by leveraging direct input validation, edit checks and auto calculation formula to capture only clean study data.
Integrate and harmonizing data from multiple sources by connecting all clinician, patient, and device data at an individual record level. Clinvigilant’s electronic data capture (EDC) system directly integrates eSource, eCRF, ePRO/COA, Laboratory and device data.
Clinvigilant EDC Highlights
Manage Phase I – IV studies
Design eCRF with Multilingual
CDASH – CIDSC based Global library
Medical Coding tool
Set Dynamic Workflow and Patient Scheduling
Clinvigilant EDC Modules
Manage single site or multi sites
Manage Site Team
Manage Role Access
Manage Rules and Formula
360 Degree view of Subjects
Manage Query / deviations
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