Solutions

HMD's Clinical Trial Management Suite is a 24x7, multi-lingual IVR and Web based solution

Trial management

• Site feasibility and initiation
• Online site and subject surveys
• CRA monitoring
• Subject maintenance
• Site/users maintenance
• Patient diaries
• Regulatory document management
• Track regulatory milestones
• Reduced paper flow

Trial control

• Screening
• Enrolment
• Randomisation
• Dispensation
• Adaptive design
• Emergency break blind
• Withdrawal or completion

Trial reporting

• Real time tracking and reporting
• Automatic email notifications of study and site progress
• Exception alerts
• Inventory reporting
• Automated, scheduled reporting

Drug supply management

• Start trial with minimal supplied
• Reduction in drug waste at investigator sites
• Reduction in storage of drug required at site
• Track expiration dates and batches
• Recall and reconciliation of expired or damaged materials
• Shipping documentation generated
• Automated shipment generation based on actual or estimated requirements at sites
• Forecasting and tracking of drug supply requirements