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 Life and other standardized questionnaires:
- Provide author, copyright holder, or contact information to gain Permissions for Use
- Determine validity and historical usage
- Identify the ideal measurement strategies for your study: Population, endpoints and minimally clinically important difference (MID)
- Identify the most appropriate measurement strategies for your study (population, endpoints and MID (minimally clinically important difference)
- Access supporting information to include in regulatory dossiers
- Assist in design of customized ePRO reports
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