Run Clinical Trials at speed - without compromising on quality.

What to expect from a conversation:

  • You’ll share your goals and the challenges you wish to overcome.

  • You'll learn how we can address your needs to help you run faster, higher-quality, and significantly more affordable clinical trials.

  • You'll see data that backs this up.

  • We'll discuss the next steps.

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What our customers say

"The system was very easy to use. Even without training, we could follow all the processes and complete tasks with ease."

Prof. Dr. Emmanuel Roilides
Hippokration general hospital

"The intuitive user interface simplifies and guides the protocol development process, removes many of the review and revision issues inherent in document based approaches, ensures all required information is obtained, and most importantly, enables medical and clinical staff to focus on the research goals and clinical aspects."

Dr. Andrew Richardson
Zenetar (formerly MSD)

Carelane by the numbers

50%+

Faster Amendments

Digital Protocol
Development

Structured FHIR protocols synchronise automatically across systems, accelerate amendments through version control, and enable advanced direct data capture via standardised interoperability.

50-80%

Time Saving

Site Data
Entry

Process-first workflows and user-friendly interface reduce data entry time from 6 to 1 hour per patient.
Enjoy superior site-satisfaction due to Carelane's ease of use.

70-90%

Time Saving

Site Support & Communication

Real-time data visibility and integrated platform reduce support effort from 20 person-days to 1 person-day.

up to 80%

Cost Reduction

Total Study
Costs

Streamlined consents, simplified workflows, and reduced practitioner burden double participant numbers.

70-90%

Time Saving

Query
Management

Intelligent edit checks minimise queries while AI-assisted resolution reduces response time from weeks to days.

60-90%

Time Saving

Site Selection & Self-Registration

Automated self-registration workflows and integrated feasibility assessments reduce site selection from 10 weeks to 1 week.