IQVIA Clinical Insights
What is it?
Low-code registration platform that allows the collection and analysis of RWE (Real World Evidence) data, disease-specific and ready for research, on any device with internet access, in a Software as a Service (SaaS) or subscription model. Data can be collected directly by clinicians, patients themselves, or both, according to their access levels.
Value proposition
Structured records and look and feel designed for use by clinicians (CRD – Clinical Reported Data) and patients (PRD – Patient Reported Data). The two information collection environments can be separate or integrated into one.
Autonomous configuration and study management. Ability to supervise data quality and integrity, report recruitment, execute ad-hoc reports, validate audit logs, and export data.
PASS (Post-Authorization Safety Study) and PAES (Post-Authorization Efficacy Study)
Autonomously configurable eCRFs (electronic Case Report Forms)
Dedicated communication channel between clinician and patient
Dashboard for registered data analysis
Multicenter security, with data pseudonymization
Compliant with GDPR and certified by ISO 27001