• Introduction
  • Experience
  • Project Management
  • Quality
  • Locations
• IVRS / IWRS - IXRS
  • IXRS Features and Client Benefits
  • IXR Express
  • Dynamic Patient Randomisation and Dosing
  • Patient Tracking & Management
  • Clinical Trials Materials Management
  • Clinical Supply Management
• Reporting
  • Features
  • Suites of Reports
• ePRO
  • Why Use ePRO?
• Statistical Services
  • Dynamic Patient Randomisation & Dosing
  • Adaptive Trial Design
  • Psychometric Services for ePRO
• Web Drug Reconciliation
• Data Integration & Reporting
  • Reporting
  • Ad-hoc Reporting
• Clinical Hotline
• Technical Support

Adaptive Trial Design

Almac’s suite of technologies is one of the first comprehensive solutions to seamlessly implement and support adaptive trial design. Well-designed adaptive trials result in lower drug development costs, reduced time to market, faster go-no-go-decisions, and improved patient safety.  Our IXRS and iDiary tools capture and share safety and efficacy data and make it viewable in real-time, so that sponsors have the information to take action as predetermined in the protocol. The flexibility of our integrated systems allows for seamless change implementation during the course of a trial.

Almac has experience in implementing over 100 adaptive studies, and has established the reputation as a market leader in the area.

Read some of our published articles about Adaptive Trial Design.