CRF Health’s ‘Outstanding Innovation’ with Pioneering TrialConsent® Wins 2018 Clinical Informatics News Best Practices Awards

PLYMOUTH MEETING, PA - Feb 15, 2018 - CRF Health, a leading global provider of patient-centered eSource technology and service solutions for the life sciences industry, today announced that its electronic informed consent solution, TrialConsent®, has won the 2018 Best Practices Award at this years Clinical Informatics News Awards. The Best Practices Awards program seeks to recognize outstanding examples of applied strategic innovation-partnerships, deployments and collaborations that manifestly improve the clinical trial process. The judges named nine finalists, and from that pool chose winning entries in three categories: Clinical Data Intelligence; Study Startup and Design; and Patient Data Management. CRF Health were winners of the Study Startup and Design Award. The Awards were announced at SCOPE, the Summit for Clinical Ops Executives in Orlando, Florida, on February 14. This is the second award in 2018 recognising CRF Health as a disruptive force for innovative, high value-driven health tech solutions.

CRF Healths TrialConsent is an industry-first hybrid electronic informed consent solution fully integrated within an eCOA platform. Featuring rich multimedia, tiered-learning and interactive learning assessments, the solution promotes better comprehension, compliance and retention rates while minimizing regulatory risk. Extending the TrialMax® platform, TrialConsent features a proprietary design tool to facilitate collaboration between sponsors, research sites and IRBs/IECs while streamlining consent development, approval and deployment. The technology ensures patients receive consistent, up-to-date and accurate information, while enabling remote monitoring of the process through real-time dashboards. The solution also tracks and time-stamps interactions, supporting better documentation for each consented participant. TrialConsent can be fully integrated with existing eCOA solutions or delivered as a stand-alone solution.

Commenting on the award recognition, CRF Healths CEO, Rachael Wyllie said: Electronic methods of informed consent reduce some of the most cited regulatory deficiencies. With TrialConsent, weve worked alongside sponsors, sites and IRBs to understand their needs and to develop an intuitive eConsent platform that is robust and reliable, yet incredibly easy-to-use, and we are delighted that our solution has been selected as a winner in the 2018 Clinical informatic News Awards. Wyllie added: As an industry-first hybrid solution, TrialConsent makes the informed consent process more effective and more efficiently streamlined for all stakeholders. By allowing trial designs to easily integrate electronic informed consent and eCOA solutions on a single platform and even on the same device, TrialConsent removes the need for a separate consenting technology, significantly reducing complexity for researchers.

For further information on CRF Health and the TrialConsent solution, please visit www.crfhealth.com.

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Enclosed- Photo captioned: CRF Healths Business Development Executives, Rob Rutz, Associate Director, (left) and Gordon Row, Senior Director, (right) receive the 2018 Clinical Informatics News Best Practices Awards.

About CRF Health

CRF Health is the leading provider of patient-centered eSource for the life sciences industry. With experience in more than 800 clinical trials, over 100 languages and across 74 countries, CRF Healths TrialMax® platform consistently demonstrates the industrys highest data accuracy, patient and site compliance, and patient retention. The integrated TrialMax platform includes eCOA solutions for collecting PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes), ClinROs (Clinician or Rater Reported Outcomes), and PerfOs (Performance Outcomes), and features TrialConsent®, an electronic solution for collecting and managing informed consent in clinical trials. CRF Healths eSource solutions improve trial engagement by making the patient the center of the clinical trial process.

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