CRF Health updates ePRO software suite with TrialMax® 4.0

June 22, 2009 Naor Chazan

Lansdale, PA – June 22, 2009: CRF Health, the electronic Patient Reported Outcomes (ePRO) solutions company, today announced new functionality and enhancements to its ePRO software suite with TrialMax® 4.0.

The TrialMax eDiary design tool, Trial Studio® is the only ePRO software solution on the market that enables a truly collaborative approach to the eDiary design process. The “no manual programming” approach of the design tool permits real-time development together with the trial sponsor, giving all involved parties complete visibility and input to the eDiary design. This unique approach allows study teams to assess the usability of their eDiary design during the design phase, so that issues are found early in the process - resulting in a more streamlined deployment.

Adding to the real-time design capabilities, CRF Health’s TrialMax® 4.0 now includes automated email notification and messaging, helping site users react faster to specific events such as low subject compliance or potential safety concerns. Other additions include enhanced user account and password management features, configurable data exports in a variety of output formats, report content export to Microsoft® Excel, enhanced report printing and configurable patient status icons.

The TrialMax® 4.0 has also been updated with new user interface graphics and the ability to embed links in study reports. With this new version, the TrialMax system was upgraded to run on the latest releases of the Oracle® database and WebLogic® application server.

Rachael King, CEO, CRF Health, said: “We recognize that the ePRO data collection needs for investigator sites and patients are varied and complex. TrialMax® 4.0 has been developed to provide rich and validated functionality, allowing sponsors to collect primary and secondary efficacy data faster and with greater flexibility“.


About CRF Health

CRF Inc. d/b/a CRF Health is the global leader in ePRO (electronic Patient Reported Outcomes) solutions for the life sciences industry. Through innovative technology, a thorough understanding of drug development and mobile computing, CRF Health is driving the change to higher quality outcomes and more efficient paper-free clinical trials.

CRF Health’s ePRO technology has been used in more than 60 countries, on six continents and 68 regional languages, including ten regional Indian dialects.CRF Health consistently demonstrates the industry’s highest patient compliance rates while delivering unrivalled data accuracy and unmatched patient and site acceptance.

Since its founding in 2000, CRF Health continues to provide true global ePRO delivery and service. Headquartered in the US, CRF Health operates its R&D center of excellence in Helsinki, Finland and has offices around the world, including London and South Africa.

TrialMax®, TrialCollector®, TrialIntegrator®, TrialManager® and TrialStudio® are registered trademarks of CRF Health. All rights reserved. TrialLibrary™ and other CRF product references are either a trademark or service mark of CRF Health. All rights reserved. All other trademarks and/or service marks are the property of their respective owners.

For more information, please visit

Media Contact
Heather Bilinski, Marketing Manager
CRF Health
4000 Chemical Road, Suite 400
Plymouth Meeting, PA 19462
Phone: +1 267.498.2349 | Fax: +1 215.565.0001

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