Offer your patients access to novel treatments 18-24 months faster and enhance medical visibility for HCPs early on. Optimize scientific dialogue with the support of real-time, descriptive dashboards while an RWE study is still underway. Our platform supports your pharma and biotech trials – from Phase I-IV to interventional or NIS to RWE.
Clinical data capture is time-consuming and expensive. Delays in clinical trials, often triggered by slow patient recruitment, high drop-out rates and manual processes, can cost pharmaceutical companies millions every day.
This is where Climedo comes in: Our digital, cloud-based solutions help you save valuable time, create transparency for all stakeholders and improve your data quality at the same time. We're here to support you in your phase I-IV studies, interventional or non-interventional studies and the collection of real-world data (RWD).
EDC
Cost-efficient, automated and scalable: Capture data for your clinical studies and surveys electronically with our EDC system – all in one place.
Our EDC System
eCOA & ePRO
Convenient, secure and fast: Digitally capture all data reported by your patients in the course of a clinical study – on any device and with no app.
Our ePRO SolutionsReal-Time Dashboards
Our interactive dashboards enable you to see real-time visualizations of your clinical trial data and compare patient cohorts across different sites.
Our Real-Time DashboardseConsent
Simplifies your administrative processes at the start of a study. Study participants are informed digitally.
Our eConsentHybrid Trials
Implement clinical trials in a patient-centered, flexible, and decentralized manner, during the pandemic and beyond.
Our Hybrid Trial Solutions
We'll show you how to start a clinical trial or survey and address your specific needs and desires.
Climedo's intuitive user interface means you'll be onboarded in just a few hours, without the need for programming skills. Get started with your project right away.
Patient centricity and decentralized study designs accelerate your recruitment and increase patient compliance by up to 90%.
Predefined workflows with complex decision trees including automatic plausibility and validation checks improve the data quality from the time of input.
Achieve significant time savings of up to 49% thanks to reusable form templates and the possibility of decentralized study designs and remote monitoring.
Our cloud-based solution has been tested by state authorities and offers a granular roles and rights assignment for different system users.
Dashboards and smart filter views allow you to view all results in real time and thus anticipate potential problems. Data exports are possible in common formats.
Study sponsor of a pharma study
Thanks to the simple handling (independent of location or device), the intuitive usage and the automated reminders, you'll see higher participation and completion rates.
Direct patient feedback and paperless data collection will improve your data quality. With Climedo, the error-prone transfer of paper to Excel sheets and illegible handwriting become a thing of the past.
Faster results thanks to automated processes, reusable forms and decentralized study designs as well as remote monitoring.
