Acceliant Demonstrated EDC and EPRO Integration at 2012 SCDM Annual Conference

Acceliant, a global technology provider of innovative solutions in clinical trials, demonstrated "Integration of Patient Reported Outcomes (e-PRO) through multi-modal data capture with the power of EDC".

Virginia, Herndon (I-Newswire) October 3, 2012 - Acceliant, a global technology provider of innovative solutions in clinical trials, demonstrated "Integration of Patient Reported Outcomes (e-PRO) through multi-modal data capture with the power of EDC" at the 2012 SCDM Annual Conference held at Los Angeles, CA from 22 to 25 September. Acceliant was a Platinum sponsor of the conference, which is the world’s largest educational event for clinical data managers.

Acceliant is passionate about healthcare and focuses on leveraging technology to impact the way trials are managed in the industry. We contribute in an environment that is being simultaneously affected by dynamics such as regulatory change, globalization, recessionary effects, reductions in spending, and the need for predictability in trial management.

Speaking of the event’s success, Ven Thangaraj, CTO of Acceliant, said, “We would like to extend our thanks to all the attendees of the event and of the demo for making it a roaring success for us. We appreciate the interest shown in our product.” Acceliant’s single e-PRO/EDC system offers a superior solution by allowing all the study data to be readily available, eliminating the integration costs. Acceliant is passionate about healthcare and will continue to focus on leveraging technology to impact the way trials are managed in the industry.

Acceliant eClinical Suite

Acceliant eClinical Suite is competitive in meeting the challenges of today's dynamic market conditions. The Acceliant eClinical Suite is a preeminent offering that continues its 11-year expertise in providing innovative solutions for the life sciences industry. The Acceliant eClinical Suite is robust, scalable, and flexible. It has been proven by more than 350 Phase I-IV trials, covering all therapeutic areas and medical device trials. Engineered for agility, our service model differentiators enable us to easily implement and deploy solutions in response to data, functional, and analytic needs of clinical trials.