Vial EDC + eSource Features

Hosts the EDC system in the cloud and provides data security

Sets up and determines designated permission levels for users

Auto-generates or simplifies the manual addition of queries that require action in order to lock data

Eases the export of clinical data for tracking and reporting purposes

Facilitates the creation and storage of electronic case report forms and templates

Tracks history of and any changes made to eCRFs or captured data

Provides 1 or more methods to electronically collect clinical trial data

Manages patient enrollment and study randomization

Ensures compliance with regulatory requirements like 21 CFR Part 11

Provides oversight on site-specific details, participation status, enrollment planning, and site communications.

Coordinates, tracks, monitors, and manages participants enrolled in upcoming or ongoing clinical trials.

Consolidates and centralizes study-relevant data and information.

Gathers and collects contact information for trial participants.

Coordinates, tracks, monitors, and manages upcoming or ongoing clinical trials.

Records and administers study- and site-specific documents, forms, and activities.

Enables continuous and up-to-date reporting during studies.

Allows customization of study's key dates; tracks deadlines and milestones; issues progress reports.