The Company

Acceliant has been providing Clinical Data Management solutions since 1999 to clients in the CRO, medical device, pharmaceutical, biotech, and non-profit drug research industries. With fully integrated eClinical Suite, mobile-enabled ePRO, multi-lingual capabilities and 21 CFR Part 11 compliance, Acceliant has supported hundreds of trials worldwide in dozens of therapeutic areas for global giants as well as emerging healthcare innovators.

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Unified Trial Builder

Utilizing the UTB, development of case report forms for all platforms supported by Acceliant is quick & efficient

Document Management

Acceliant's built-in document management function allows study designers to increase trial flexibility

e-Patient Reported Outcomes

Acceliant team help companies electronically collect data directly from the patient, caregiver, and/or clinician

Comprehensive EDC

Acceliant team recognizes the need for a comprehensive EDC system that stays current with technology and user needs

Trial Management

Acceliant's Trial Management module provides a fully integrated, comprehensive, global solution for clinical trials


With more than a decade of experience serving Fortune 1000 to emerging clients, we ensure customer delight' mantra runs throughout Acceliant. Services are never an afterthought nor are they a means to create additional revenue from customers.

Operationalization and Integration
Operationalization & Integration

These services are designed to facilitate a better understanding of customer needs helping users adopt Acceliant platforms


Unlike most clinical trial management systems, Acceliant has a fully integrated Learning Management System (LMS)


Acceliant services team is ready to meet all your EDC needs to successfully deploy, operate, and close studies

Acceliant Trial Migration Services
(248) 383-0310

Acceliant provides Trial Migration Services to all customers worldwide

(331) 757-0000
(734) 354-1479

Acceliant customers have the option of hosting our platforms on their data center