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Build and ship studies on a single, collaborative platform.

Join the world’s first AI-powered hub for clinical research.

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Live on
6
continents
Deployed in 
50+
countries
Used by
170+
sites

Carelane is reimagin­ing how clini­cal re­search gets done—with AI-­powered tech­nology that breaks down the data and human silos holding studies back.

Key Benefits of Carelane

Carelane is an AI-native clinical research platform that unifies protocol design, data capture, and team collaboration—enabling faster study startup, better data quality, and significantly lower costs

Higher Data Quality

Real-time monitoring, standardized collection, and automated validation

Faster Execution

AI-driven processes, reduced manual work, and better team alignment

Automated Study Workflows

Built-in compliance, clearer protocols, and active issue tracking

Self Service Software at Lower Costs

Fewer amendments, optimized resources, and reduced site burden

Seamless Patient Access

Support for pragmatic designs, longer durations, and broader recruitment

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User interface of Carelane software showing site managemen.
User interface of Carelane software showing participant pathway page.
Closeup shot of a hand holding a iPhone doing a Survey.

Accelerate Performance

Our AI assistant is embedded throughout the platform. Clinical teams can simplify their toolchain, automate manual tasks, and improve the stakeholders and user experience.

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Impenetrable PHI Encryption

We secure your PHI with zero-knowledge encryption. Each piece of data has a unique key, isolated by study and site. Only authorised site members hold the keys - not Carelane, not sponsors.

Precision Access,
Perfect Control (RBAC)

We use Role-Based Access Controls (RBAC) to meticuously sculpt user's access on a strictly need-to-know basis. With Carelane you gain surgical control over data visibility.

Architectural Data Isolation

We architect unique, segregated data collections for every client, study, and site. Encryption keys are stored in a separate key-fortress, ensuring your information is uniquely secure.

Start building instantly

with an intuitive development environment with your entire study team.

Build any study

Manage concepts, protocols, and study designs all in one place.

Deploy on demand

Start your clinical trial at any time using integrated EDC, eCOA, eConsent, reporting and many more features.

Use the templates you love

Import any templates into Carelane and use your best in class document blueprints and workflows.

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User interface of Carelane software showing participant pathway page.
User interface of Carelane software showing participant pathway page.
User interface of Carelane software showing template page.

Empower Clinical Operations at Scale

Connect teams, streamline workflows, and 
accelerate clinical trials from end-to-end on a single, integrated platform.

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Unified Planning & Tracking

Coordinate studies across the full lifecycle, from protocol authoring to conduct, with real-time data insights.

Collaborate in Real-Time

Plan effectively with adaptable tools that sync with your processes and centralize tasks, data, and vendor partners.

Your Workflows, Your Way

Plan effectively with adaptable tools that sync with your processes and centralize tasks, data, and vendor partners.

Automate Tedious Tasks

Streamline operations by automating workflows across planning, data management, regulatory prep, site & patient processes, and more.

Reduce Amendments

Significantly decrease study amendments through quality by design and structured digital protocols.

Scale Globally

Confidently deploy and manage studies and teams across every continent.

Accelerate Timelines

Deploy studies faster, save quarters, and reduce budgets by regaining control of your data workflows.

Drive Innovation

Leverage integrated tools and enhanced AI collaboration for impactful participant outcomes.

Built in data security

Safeguard participant data with robust, built-in security measures. Easily manage user roles and permissions to ensure data is accessed only by authorized personnel.

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Mark data fields as sensitive in seconds. Accelerate regulatory reviews and IRB approvals to launch your studies with the highest level of security built-in from the start

Ready to try Carelane?

The only end-to end solution for observational trials.
Unlock research at scale, slashing costs, complexity and friction!

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