Clinical Research Study Registry Features Workflow
Manage clinical trials through a centralized registry, featuring study design, protocol development, participant recruitment, data management, and outcome reporting.
Clinical Research Study Registry Features
Send Email Notification
Save Study Design Information
Update Investigator Brochure
Create Protocol Amendment Task
Send Email Reminder
Save Regulatory Agency Approval
Update Clinical Research Study Registry Features Checklist
Create Task for Sponsor Notification
Send Email Notification to Stakeholders
Clinical Research Study Registry Features
Type: Fill Checklist
The Clinical Research Study Registry features enable streamlined management of research studies throughout their lifecycle. This module provides a centralized platform for investigators to create, manage, and track the progress of their clinical trials. Study creation involves filling out a detailed online form with essential study information such as title, objectives, patient population, study design, interventions, outcomes, and contact details for principal investigators and sponsor organizations. Once submitted, studies are reviewed by site administrators who verify the accuracy of provided data. Approved studies become visible in the registry, allowing other researchers to search, browse, and access detailed information about ongoing clinical trials. The system also facilitates the submission of protocol amendments, which are subject to review and approval prior to study continuation or initiation
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