Why Use Almac for ePRO?
Increased Compliance • Patient compliance rates exceeding 90% using IVRS • Automated patient reminder via email, phone, or text • Customized compliance and other alerts for study personnel • Support regulatory submissions for new drugs, label changes, and label claims Accurate, Secure Data • Fully redundant, multi-layered secure database, telecommunication, and network • Time and date-stamps for all patient data entry provides high quality data regulatory authorities require • Logical queries and data checks reduce the likelihood of data entry errors • Real time access to patient data allows for timely identification and implementation of mid-study changes • CDISC compliant systems • Data transfers available in SAS, ASCII, XML, Excel and other formats using SFTP (SSH 2), VPN, SMTP, or HTTPS transports Statistical / Psychometrics Services • Consultation for identification of the most favourable measurement strategies for your trial • Literature searches to assist in use of Quality of Li
