Save time and money on your next clinical trial with our EDC solutions, such as eCRF, eCOA/ePRO, and eSurveys. Trusted in 200+ projects at ~3,000 sites, with more than 2 million patients and 90+% patient adherence.
ADC
At the center of everything
Everything else builds on it. Autonomous Data Capture (ADC) brings study data straight from sources such as documents, scans, voice and connected systems into the EDC, instead of typing it in by hand. People review and confirm, and every step stays traceable.
See How ADC Works
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 SystemeCOA & 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 &
Televisits
Enrol participants wherever they are: they read and sign the consent on their own device and, when needed, meet the study doctor in a televisit.
Our eConsent & TelevisitsHybrid Trials
Patient-centered and flexible: Combine visits at the site with ePRO and televisits from home, so patients can take part wherever they are.
Our Hybrid Trial SolutionsThe modules above are not separate tools. Sites, labs, patients, hospitals and pharmacies feed one platform. ADC turns whatever arrives into one validated study record, and sponsors, data managers, HCPs and patients all work from that same record.
1Capture
eCRFs and eConsent at the site, ePRO and eCOA from patients at home, lab results, EHR data and dispensing records. Nobody re-keys values from paper or PDFs.
2Harmonize
ADC maps each value to its eCRF field and converts units. A person approves the import, and the audit trail records where every value came from.
3Use
Sponsors follow the study in live dashboards, data managers handle queries and SDV in one place, and HCPs and KOLs see the evidence while the study is still running.
PD med. Lena Oevermann
Assistant Medical Director of Department of Pediatric Oncology and Hematology at Charité
Christiane Weis, M.Sc.
Clinical Department, GELITA MEDICAL GmbH
Dr. Jens Milde
Managing Director Project Delivery, Astrum CRO Germany (formerly Pharmalog)
Case Study
Dr. med. dent. Wolfgang Maas
Oral Surgeon, Implantology Practice
Prof. Dr. Christoph Schmitz
Chief Medical Officer, Auto Tissue Berlin
Case Study
From Phase I–IV and non-interventional studies to real-world evidence: sites capture data with less effort, and your medical teams see real-time insights while the study runs.
Run clinical investigations, PMCF studies, registries and surveys for medical devices and SaMD in line with EU MDR, on one validated platform.
Set up studies for your sponsors in days with the AI Study Configurator, and deliver clean data with less work for sites.
Run investigator-initiated studies and registries on a secure, GDPR-compliant platform that your team sets up without coding.