Adaptive trial design
Acceliant designs clinical trials studies for medical device enterprises accounting for changes of new data without compromising the integrity of the study. We provide seamless form versioning for case report forms (CRF) and deploy the new version, thereby allowing each site to migrate to the latest version.
Device trials design and outcomes
Acceliant leverages rich experience in medical devices to define the road map of the medical device trials design. Our team is focused on delivering primary and secondary outcomes by implementing processes across the lifecycle of the trials.
Regulatory compliance
Acceliant’s Clinical Data Management System (CDMS) accelerates study design and deployment of medical devices. We offer a complete audit trail of activities during medical device trials. Our services comply with the United States Food and Drug Administration (FDA) Code of Federal Regulations (CFR) 21 Part 820 and the International Organization for Standardization (ISO) 13485:2003 guidelines for medical devices.
