Navigate clinical trials
Acceliant leverages rich experience to simplify the processes of clinical trials. We design trials to deliver outcomes while addressing the requirements of Sponsors, regulators, and payers.
Regulatory compliance and governance
Our information security and network policy safeguards the integrity of your clinical trials data. We ensure that the clinical data of bioavailability / bioequivalence studies complies with Clinical Data Interchange Standards Consortium (CDISC) standards. Our cloud 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.
Acceliant enables researchers to manage data and use it to their advantage during clinical trials. We implement best practices in database management to help researchers dice and analyze data, and generate reports with insightful information.
Training and support
Acceliant helps CROs accelerate adoption of a clinical data management system (CDMS) with a robust training methodology. We expedite onboarding of your team using a proprietary learning management system that facilitates continuous training and support.