OneClinical
Manage your clinical trials efficiently with our
AI platform- OneClinical
Gain Value from OneClinical, our AI Driven
Technology Platform

Faster identification of trends for rapid, proactive issue resolution

Enhanced site effectiveness

Data Quality Improvements

Enhanced medical and risk-based monitoring

Successful Outcomes
Get in touch
Be a Market Leader using Insights Driven Decision Making through Analytics
Our eClinical platform enables end to end clinical trial data management, data visualization, analytics, monitoring and submission services. Proven across a variety of global trials, the platform offers short setup time with low fixed costs and provides global accessibility with near real-time data analytics and visualizations.

OneClinical Delivers Outcomes
Your clinical trial needs our carefully designed AI platform

Designed for, and delivered via, cloud, and in compliance with regulatory and data privacy requirements, OneClinical provides quality by design, effective oversight of trials and actionable insights through comprehensive data visualization. OneClinical reduces source data verification through industry standards driven central, remote and risk-based monitoring, and enables data review, query reconciliation and management through a configurable workflow based solution.
Why you need OneClinical
for your Clinical Trial

Better oversight

Global trials management

Near real time data

Informed decisions

Minimized Risk

Successful outcomes
Navitas Life Sciences
is named as a Major Contender
in Everest Group’s
Clinical Development Platforms Products
PEAK Matrix® Assessment 2022
Empower your clinical trials
Run Better Clinical Trials with OneClinical

Rapid data integration

Faster and informed decision making

Improved operational efficiency
OneClinical Features
Data Capture / Acquisition
- Site Friendly
- SmartLinks – creating a more efficient workflow for each user
- Field level edit checks and edits, including cross–panel logic checks fire immediately on data entry
- Simplified Randomization, Subject Enrollment and Drug Supply Management
- Latest statistical methods, programming and validation procedures
- Online investigator visit monitoring reports
- Workflow e–Signature authority


Data Aggregation and Analytics
- Source System & Data Format Agnostic
- Machine & Deep learning algorithms
- Document–oriented database
- Robust Mapping Engine
- Interactive visualization TransCelerate, MCC and custom RACT Plans
- Adaptive Monitoring Capabilities
- Definable Risks parameters
- Actionable Insights
- Integrated Subject Review
- Cross Study oversight
Data Submission
- Consistent and Predictable time/effort from Study Creation to Define XML
- Facilitates Use and Re-Use of existing/previous Study and Project Metadata
- Define XML can be ‘quickly’ generated for single datasets or multiple
