![Surviving-an-FDA-GCP-Inspection-500.jpg Surviving an FDA GCP Inspection](https://www.centerwatch.com/ext/resources/products/Surviving-an-FDA-GCP-Inspection-500.jpg?height=200&t=1605810958&width=200)
Home » Cliantha Research selects Acceliant for trial data management
Cliantha Research selects Acceliant for trial data management
February 27, 2013
Acceliant, a global technology provider of clinical trial data management solutions, has been chosen by Cliantha Research, a global CRO, to provide its eClinical Suite for Cliantha’s clinical trial data management needs. Acceliant's integrated e-PRO system offers a superior solution by allowing all the study data to be readily available, eliminating the integration costs.
"We evaluated and selected Acceliant eClinical Suite because we found it to be very user-friendly and superior to several other products,” said Hitesh Chauhan, associate director of biometrics, Cliantha Research. “Besides being a platform with best-in-class features, Acceliant's eClinical Suite is architected process and system wise to drive efficiency, lower costs and accelerate clinical trial studies."
Ven Thangaraj, CTO of Acceliant, said, "The life sciences industry is going through dramatic changes and pressures to innovate while keeping costs under control. Acceliant is one of the few integrated EDC-ePRO platforms with innovative workflows and built-in mobility which allows data management from anywhere, anytime."
Upcoming Events
-
21Oct