Federated real-world data registries, built with hospitals and clinical leaders.
Registries that combine hospital records with data patients provide directly, on a federated architecture where each hospital keeps control of its own data.
A trusted third party framework makes it possible to compute on non-anonymized data within EHDS and Data Governance Act expectations.
Steering committees of clinical leaders shape the study design, and the publication pipeline is part of the program.
Patient-reported outcome instruments completed by the participant.
Live study monitoring, data quality reports and site communication.
Benchmarking, statistical analysis and aggregated reporting.
Site exports, custom sponsor exports and raw data export.
Legal and technical framework for compliant computing on non-anonymized data.
PROM, medication use, side effects and interventions captured as structured registry input.
24/7 multilingual support for participants, sites, caregivers, CROs and sponsors.
Participant-facing content in the languages a study runs in.
A single point of contact from start-up to database lock.
A named data manager through to database lock.
Site initiation visits, investigator meetings, site training and train-the-trainer.
Tell us what you are working on and we will point you to the right people.
