Driving Simplicity in Clinical Research
Carelane is a groundbreaking HL7 FHIR-based platform that revolutionizes real world evidence research by enabling seamless study design, execution, and analysis.
Don’t take our word for it. See what our clients say
80% cost saving in study setup and site management compared to previous study
“The study setup was highly intuitive and the time we saved on site selection and onboarding was impressive. By adapting the Carelane workflow templates and adding them to our study setup, we only needed to send out one email; everything else was automated. Our team quickly grasped how to build our case report form, which included complex fields with conditions and calculations. What really made a difference to me was the ability to invite collaborators and reviewers, it allowed them to comment on each individual item and accelerated the study setup tremendously.”
“The study setup was highly intuitive and the time we saved on site selection and onboarding was impressive. By adapting the Carelane workflow templates and adding them to our study setup, we only needed to send out one email; everything else was automated. Our team quickly grasped how to build our case report form, which included complex fields with conditions and calculations. What really made a difference to me was the ability to invite collaborators and reviewers, it allowed them to comment on each individual item and accelerated the study setup tremendously.”
Prof. Dr. Martin Hoenigl
President of european confederation of medical mycology (ECMM) Medical university of Graz
70% time saving in data management compared to other studies on site
“The system was very easy to use. Even without training, we could follow all the processes and complete tasks with ease.”
80% time saving compared to status quo (measured on several aspects of protocol development with two comparable studies)
“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”
“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)
Simplifying the Entire Clinical Trial Process
Study Authoring & Planning:
Simplify the entire study design process with tools to define evidence, rationale, cohorts, objectives, and endpoints, while fostering seamless collaboration and efficient document management.
.svg){kind=icon}
Site Management & Study Operations:
Optimize site and participant workflows with powerful tools for partner management, onboarding, data capture, and monitoring, ensuring smooth and compliant study execution.
Analysis & Reporting:
Gain actionable insights with advanced analytics, automated reporting, and seamless data extraction, empowering faster decision-making and regulatory submissions.
The only platform you need
Scalable Self Service Platform
Carelane is as powerful as you need it to be, supporting everything from small studies to large-scale studies spanning multiple continents—all on one platform.
Process Coordination
Efficient process management, automated workflows, and clear communication channels to optimize the operational efficiency of your research projects.
Study Design
Comprehensive study design capabilities, including textual protocols, endpoint definition, and eligibility criteria management, to ease the planning of your research studies.
Participant Management
Intuitive management and tracking with detailed data recording to optimize the monitoring of your study participants.
Data Governance
Secure storage solutions and real-time analytics to enhance the integrity and accessibility of your study data.
Site Operations
Streamlined site management, centralized coordination, and compliance tracking to empower your research sites efficiently.
