Evado Clinical
Clinical data management for trials, studies, and registries with electronic data capture, monitoring, and multi-site coordination.
Overview
Evado Clinical is a cloud-based platform developed by Evado, a Melbourne-based technology company with over 30 years of experience in mobile-enabled solutions. The platform manages clinical data for clinical trials, studies, and registries, and is developed, hosted, and supported in Australia. It is designed for sponsors and research organisations running trials of any size, from small studies to large multi-site registries.
Evado Clinical meets the regulatory requirements of FDA 21 CFR Part 11, HIPAA, and the International Council for Harmonisation Good Clinical Practice (ICH GCP) E6. The platform provides a fully integrated environment that allows customers to run multiple trials, studies, or registries across multiple sites simultaneously.
Key Features
- Run an unlimited number of trials and studies simultaneously within a single environment.
- Online record layout tools for data collection.
- Standardised, configurable layout field validation rules.
- Online record review, monitoring, and data management.
- Scheduling support for multiple-arm trials.
- Online data query functionality.
- Statistical export of data.
- Registry data records.
- Case Report Forms (CRFs).
- Questionnaires and standardised data collection instruments.
- General record layouts including Adverse Events (AE), Serious Adverse Events (SAE), and Concomitant Medications.
- Each record layout is versioned and can be updated at any point during a trial.
- External images and streamed videos can be included in form layouts.
- Accessible from a standard web browser or mobile device.
Platform Benefits
- Easy to learn and use.
- Trials and studies can be quickly deployed.
- Simplifies trial record management.
- Easy creation and completion of records.
- Record layouts can be reused across multiple clinical trials.
- Transparent pricing on a per-trial basis.
- Fully integrated environment.
Service Tiers
- Lite: Designed for small trials with a maximum of 200 subjects. Includes electronic informed consent (stand-alone or integrated with EDC), one schedule, remote trial participation, remote monitoring, simple scheduling and data collection, and web-based Clinical Outcome Assessment (COA) functionality.
- Standard: Designed for medium-sized trials or registries with a maximum of 500 subjects. Includes all Lite features plus eSignature, eSource, multi-arm trials, randomisation, and web and device eCOA functionality.
- Enhanced: Designed for large trials or registries with more than 500 subjects. Includes all Standard functionality scaled for larger subject populations.
Enterprise Service
- Available for customers running multiple trials or registries.
- Supports web service integration with external systems or services.
- Informed Consent can be run as a stand-alone trial or integrated with the EDC component.
Evado Clinical is priced on a per-trial basis across its three service tiers, and is positioned to support fast turnaround from trial setup to recruitment. The platform is hosted in Australia and is designed to deliver enterprise-level functionality as an on-demand service.


