Clinical development

Run efficient, cost-effective clinical trials that get treatments to market faster. Already a user? Log in to Merative Clinical Development.

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A clinical data management and acquisition system that puts you in control.

See why 3,400 studies in 109 countries have run on Merative Clinical Development.

Flexible and scalable

Control any clinical trial – regardless of phase, therapeutic area or geographical location. 

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Easy to use

Implement and execute research, manage participant compliance, perform routine tasks and report results – all through a single, user-friendly interface.

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Accessible anytime, anywhere

Use single sign-on to access the solution from anywhere in the world.

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FEATURES

Modernize your clinical development experience

 

Improve efficiency with integrated modules and functions – accessible within one solution and built on a single code base.

eConsent

Empower participants and caregivers to deliver consent and enter data – in real time, from their own devices.

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Data integration

Integrate into third-party solutions with minimal coding.

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Reporting and analytics

Use pre-built and custom reports that uncover hidden insights – and lead to better decisions.

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Medical coding

Validate medical coding quickly with the help of artificial intelligence (AI).

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Randomization and trial supply management

Manage randomization and trial supplies without complex coding.

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Endpoint adjudication

Compile clinical trial endpoint details and source documents at the push of a button.

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CASE STUDIES

Improving clinical trials

Learn how Biorasi reduced costs, overhead and time with our clinical data management system.

Increasing efficiency

Learn how Veristat gained efficiency and control over its clinical trials.

Scaling quickly

See how George Clinical was able to serve its expanding clientele with a modular clinical development solution.

Getting to market faster

Find out how ProTrials is accelerating processes across the development life cycle.

Enhancing productivity

Learn how Prosciento is using AI to complete medical coding with speed and precision.

RESOURCES

Dig deeper into clinical development

SOLUTION BRIEF

Clinical development for CROs

Learn more about features for clinical research organizations designed to promote self-sufficiency as well as study setup and execution.

SOLUTION BRIEF

Clinical development for medical devices

Explore features unique to medical device trials, including assistance with MDR and 510(k) and fully-integrated DICOM capabilities.

SOLUTION BRIEF

Clinical development for pharmaceutical organizations

Explore features like electronic data capture, electronic clinical outcome assessment (eCOA) and randomization and trial supply management (RTSM).

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development expert

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