“Pharmaceuticals, Biotechs, and Contract Research Organizations are rapidly adopting newer technologies for Clinical Trial Management process. The need to expedite the trials while keeping them cost-effective, and being compliant to regulatory demands is driving the business decisions." says Dr. AL Rao, Board Member of Acceliant, a global technology provider of innovative clinical trial management solutions. The company has remained au courant to the developments for over a decade by observing the changes in priorities and dynamics that continue to influence the life science industry. The extensive research helped Acceliant to create a platform, which can automatically integrate, connect, facilitate workflows, and collaborate in a mobile environment. The company’s innovative solutions have been utilized in several large multinational trials with over 25,000 enrolled patients in over 15 countries. Recently, Acceliant has been ranked highest in ‘Overall Satisfaction’ amongst EDC providers in ISR Reports (Industry Standard Research Reports) publication named “EDC and eCOA / ePRO Market Dynamics and Service Provider Performance (2015)”. Terming it as a significant milestone, Dr. Rao says, "In the recent years, we have elevated our focus on understanding the industry challenges and further emphasized on strengthening the solution to meet our Client’s needs.”

The speckless innovative techniques and a touchstone technology of the decade
Acceliant’s comprehensive Clinical Data Management System (CDMS) – and the eClinical Suite, leverages latest technologies to facilitate Electronic Data Capture (EDC), electronic Patient Reported Outcomes (ePRO), Clinical Imaging Systems (CIMS) and other features to manage data in compliance with regulations. The Acceliant Unified Trial System (UTS) provides 100 percent integration between program management, trial design, data capture, data management, reports, and business intelligence. The company’s trial specific services consist of trial build, mid-trial migration and a choice of On-premise or Cloud-based hosting. The company’s cost and time effective, ‘Design Once’ and ‘Deploy Many’ trial design, provides an array of data capture options for browsers, tablets and mobile devices, in addition to eSource Electronic Ink/Pen, Barcode Registration and Identification. Acceliant also provides a user-friendly interface to enter data from a wide variety of devices in an automated or semi-automated fashion. Acceliant’s services include operationalization, and integration with the existing environment, conducting pilot study & learning, providing a fully integrated learning management system and making training current with social and business trends. Additionally, Unified Trial Builder enables the setup of a CRF within weeks using data-import technology capable of mapping and importing data across several hundred fields and scores of forms. A web-enabled Document Management System (DMS), used for organizing, versioning and maintaining the clinical trials document, offers concession in the duration of clinical trials, and enhances profitability. Acceliant also provides convenient migration frameworks for in-flight trials, delivers trial assurance, and lower total cost of ownership.

Sharpening its adroitness for future challenges
Acceliant just unveiled the latest Version 7.0 with its comprehensive suite of solutions. Derived directly from the client feedback, Acceliant v7.0 delivers enhanced usability by leveraging an improved UI, streamlining the data collection process, and driving efficiency across the life cycle of clinical trials. The newly added features include: Single Sign-on making it easier for integration; time-saving features such as Change Notification via Email/SMS; and improved Image Mapping helping users in better data visualization. To face the challenges that lay ahead, the company is investing more time and energy on sharpening its adroitness with the help of its dedicated entourage of expert minds.