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Medical Devices

Acceliant manages clinical trials to enhance the efficacy of medical devices

Medical device manufacturers partner with Acceliant to manage clinical trials and enhance the efficacy of medical devices. Our experienced team blends data analytics with advanced technology to shape the next generation of medical devices.

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.

Watch: How we add value

Want to know more? Talk to us.

Contact us+1-408-387-5800