Site Solutions
Our eCOA services and capabilities
eCOA (Electronic Clinical Outcome Assessment) solutions enable real time data collection from investigator sites on subjects participating in studies. Our solution can be used by sites on via tablets or remotely by patients using their own device and includes the following key features:
Clinical staff portal available in multiple languages.
Comprehensive Site and Patient Data.
Inform patient about the study.
Collect consent & registration form and HCP's signature.
Follow study and patient progress.
eCRF (Electronic Case Report Forms) are used in a clinical trial to record the protocol and all required information about study participants. Our tools enables to:
Build advanced eCRFs.
Deploy your study in 3 weeks on average.
Provide data monitoring and data management.
Patient Solutions
Our patient solution covers the full life cycle of patients in clinical trials from consent to day-to-day feedback:
eConsent provides patients with study information, accessible on-site via tablet or remotely on personal devices.
Collect signed documents and electronic signatures.
Enable patients to download their signed ICF.
Enable patients to review their right.
Perform patient ID verification if remotely collected.
Allow patients to withdraw consent during the study.
ePRO: capture of validated Quality of Life (QoL) surveys as per ISPOR5 guidelines.
eDiary: library of data input modules to capture exploratory endpoints.
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Bio Sensors
Bio sensors play a key role in monitoring and tracking various health parameters in real-time. Each device is designed to provide accurate, continuous data, empowering users and healthcare professionals with valuable insights for proactive health management. Our range of advanced devices includes:
More information about provisionning
Project Types
Simple electronic study design and workflow, easy to use and user-friendly interface, patient design oriented
We offer flexible and robust solutions tailored to customers’ needs and studies requirements. This enables us to provide our solutions to:
Monocentric or multicentric projects.
Healthy Volunteers – PH 1 Unit.
Late Phase Solutions: Full Service.
SAAS Model: Do It Yourself.
Benefits
Benefits of working with our e-clinical experts
Our e-clinical solutions are designed to enhance the quality and efficiency of clinical trials by simplifying patient-reported data collection. Our platform offers:
Increased patient compliance and engagement through user-friendly interfaces.
Full support from trial design to database lock, ensuring seamless project execution.
Faster data capture and cleaner datasets for improved trial outcomes.
With a flexible and multilingual system, we help sponsors and sites collect accurate, real-time data while improving the overall patient experience.
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