Manage and engage with sites directly from the system. Assign sites to a particular study and track their documentation, credentialing, equipment, facilities, and activation status. Deliver content and services to clinical research sites through the investigator portal. Provide documents to all the sites through the system to keep the sites informed and engaged.

Site Feasibility

Get Real-time visibility to all the subjects and track subject visit activities and schedules. Define the procedures, subject visits & payment policies depending upon the budgets and protocols.

Set up a monitoring schedule based on the monitoring plan and Schedule monitoring visits. Identify data discrepancies through 100% SDV or set algorithms to perform SDV on specific and relevant data items such as safety data, enrollment, primary or secondary objectives, etc. Easily set up edit checks within the system and risk-based monitoring workflows including Key Risk Indicators, triggers, and thresholds.

Use the latest version of the widely used built-in DIA reference model or use your own model. Add or remove folders from the built-in models and apply directly to a study as required by a study-specific TMF plan and index.

Find and retrieve documents using a search engine that's effective for both file names and metadata. Create custom list views with numerous available filters.

Cloudbyz eConsent replaces the paper-based informed consent document with interactive, multimedia enabled, and template-driven informed consent on mobile devices. The solution is fully integrated with Cloudbyz EDC enabling real time visibility and central tracking of enrollment metrics across the sites.

Cloudbyz EDC simplifies study setup, accelerates data collection with creation of simple to complex forms and reusable form libraries, and reduces data management costs.

Cloudbyz Safety and PV solution allows users to report adverse events, track and manage all cases from receipt to closure, and monitor progress. Attached other product screenshots as well.