Seamlessly integrate eCRF and ePRO to collect clinical data from both healthcare staff and patients.
Clinical data entry from clinicians and healthcare staff from eCRF
Combine clinical information with patient-reported outcomes, to build a solid registry around the usage and efficacy of your device
Set up advanced validation rules on individual questions.Trigger SMART-TRIAL to automatically show a warning message, create a query, or block the data input.
Enhance the informed consent process using electronic signatures.
Ready-to-use MDR and ISO 14155:2020 AE teamplate with automatic rules and notifications.