ePRO

Clinical trials can be delayed due to slow enrollment, problems with paper documentation and the inability to monitor sensitive patient data — costing sponsors millions of dollars. ERT’s ePRO (electronic patient reported outcomes) solutions enable our clients to capture sensitive findings directly from their patients, a process that is critical to proving the efficacy of their compound and its effects on patient safety.

Use of PDAs and other computer solutions involve a major commitment of capital, time and resources. ERT, however, offers a quick and easy, phone-based, voice-response solution, which is designed and optimized to help our clients collect clinically valid and sensitive data directly from participating patients.

ERT’s user-friendly, direct approach supports all key aspects of clinical trials:

• Patient recruitment
• Clinical assessments
• Monitoring and alerting (including suicidality monitoring)
• Protocol design and validation consulting 
 
At ERT, we employ our exclusive Project Assurance methodology to develop a planning roadmap at the start of your ePRO engagement. This roadmap offers a consistent framework through which we can effectively manage the delivery of all ePRO services — from patient recruitment through data delivery. We take every action necessary to provide our clients with the standards, guidelines and services that allow us to effectively and proactively manage their needs — exceeding their goals.

Additionally, ERT’s My Study Portal provides real-time access to your ERT ePRO data through a single, secure website. All of the reporting tools you need to effectively manage and track your PRO data are available, on demand. My Study Portal provides more than simple roll-up reports — offering timely access to your comprehensive ePRO data from any location.

For more information please see our website, or contact us.