MCR CLINIC™ Systems
Automation is the future of clinical research. It combines previously practiced physical monitoring visits in smaller numbers with the integration of various electronic systems. Our systems are the answer to this challenge.
We meet the highest requirements for FHIR medical information systems, HL7 medical data exchange, GDPR personal data protection and 21 CFR part 11 research
We meet the EMA guidelines for remote access to eSource data and remote monitoring of clinical trials
System for site managers and research coordinators for effective contracting, supervision and billing
System for remote study monitoring in a hybrid model for sponsors and CROs
DATA COMM. INTEGRATOR (DCI™)
System for secure and automated data exchange between different modules used in clinical trials