OpenEvidence Features

Measures the tool’s sensitivity, specificity, or other metrics in actual diagnostic scenarios.

Verifies compliance with certifications like FDA, CE, or other health authority approvals.

Offers transparent reasoning behind outputs and trackable logs for review or compliance.

Confirms clinical effectiveness based on real‑world usage or peer‑reviewed studies.

Ensures consistent diagnostic performance across demographics, sites, or data sources.

Securely stores data to prevent data loss or breaches

Alerts or notifications of various types such as pop-up messages, sounds, banners, or badges

Web form that allows users to enter data that is sent and processed for different reasons

Manage the process of evaluating documents or requests submitted for approval

Configure existing workflows to meet your organization's needs

Active reporting of data and metrics

Digitally sign online documents

Access software remotely via mobile devices

Set up connections to third-party platforms to improve business processes

Assemble applications and processes by dragging over and arranging pre-built components

Ability of websites, web applications, or mobile applications to function without an active internet connection

Add customized logos and colors to align with company branding

Use AI to generate content in the form of text, images, videos, etc.

Convert paper files into digital images

Customize data fields to support various needs and use cases

A virtual assistant that uses AI to pursue goals and complete tasks on behalf of users

Customize contracts and forms to collect specific information

Store and organize documents in a centralized system

Import, collect, and capture data from multiple sources

Graphical representation of data

Synchronizing data between two or more devices/systems and automatically updating changes to maintain consistency

Process of checking different types of data for accuracy to avoid errors or inconsistencies

Compliant with HIPAA, which sets standards for sensitive patient data protection

Alter the layout and content of reports

A record of all activities within the system, including user access, changes made, etc.

View and track pertinent metrics to find patterns and gain insights from data

Pre-designed layouts that can be customized to match preferences and requirements

Assign categories, labels, tags, or attributes to documents for organization, search and storage

Automatically retrieve and pull information from documents, websites, images, data sets, and other sources

Application programming interface that allows for integration with other systems/databases

Electronic signing method that validates the authenticity and integrity of a digital document

Dashboard to view the status of ongoing processes, identify current incidents and track past activities

Manage and support multiple languages

Offer training, documentation, and onboarding support to users.

Provide an intuitive user interface that minimizes disruption to clinical workflows.

Track performance, usage, and feedback after deployment to support ongoing improvement.

Support version updates, rollback, and clinician feedback workflows.

Complies with data protection standards (e.g., HIPAA, GDPR) and enforce secure data handling.

Integrates directly into clinical systems such as EHRs, PACS, or RIS.

Flags urgent or abnormal cases to clinicians in a timely, workflow-optimized manner.

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

Import and export data to and from software applications

Create, design and manage workflows for repetitive tasks

Track and manage adherence to policies for any service, product, process, or supplier

Tools to manage single or multiple clinical studies within a centralized platform

Store, manage, and track all electronic documents in a centralized location

Plan, schedule, and execute organization's accounts and assets to ensure compliance with policies and laws

Store, manage and track all forms in a centralized location

Manage and store data in a database

Define levels of authorization for access to specific files or systems

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

Receive data and information in real time

Capture data electronically

Uses decentralized resources such as network scanners, multi-function devices (MFD), and desktop scanners to collect data and documents