Clindex Trial and Data Management
SOLUTIONS

Clindex
Trial and Data Management

Clindex Remote Data Entry



To receive a brochure, please contact Sales.




Schedule a live demonstration

Accelerate your trial and ensure data integrity with Clindex
Offering a comprehensive set of capabilities in one complete solution, the Clindex® Clinical Trial and Data Management System is designed for trial professionals. By integrating all of the trial processes into one system, Clindex provides a seamless environment for clinical trial and data management, allowing you to:

Accelerate your trial and reduce time-to-market
By managing trial design and administration in a more efficient, expedient manner, Clindex allows your staff to manage trials without additional IT development--enabling faster trial and Case Report Form (CRF) construction. Combined with faster trial implementation due to Clindex's ease-of-use and reduced training requirements, this means faster trial execution and a reduced time-to-market.

Ensure data integrity
Providing support for 21 CFR Part 11, Clindex meets all FDA guidelines for clinical data management systems. Clindex manages all aspects of data auditing and access and allows the developers of clinical trials to concentrate on screen and form design, data dictionary and data editing.

Clindex enhances study database design, methodology and administration and streamlines data entry and tracking of CRFs, payment of CRFs and study monitoring. Clindex also provides powerful reporting functionality — from standard out-of-the-box reports, to ad hoc reporting capabilities, to data extraction for statistical analysis and study archival. With integrated functions to support all the steps in the clinical trial process, Clindex has an intuitive user interface and an open architecture to allow users and study administrators to customize their own solutions.

Download a product brochure with more information,
or schedule a live demo of Clindex Clinical Trial and Data Management.