• 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

Clinical Supply Management

Along with its sister division Almac Clinical Services, Almac Clinical Technologies offers an integrated supply chain management solution that draws from the expertise of our best-in-class clinical trial supplies and IVR / Web Based services. Our integrated solution does more than just combine related services under one roof; it incorporates supply planning, technology implementation, and project oversight into a unified study start-up and management approach that optimizes the supply chain at each level. 

Almac’s Full Clinical Supply Management offering allows clients to benefit from the following:

• Leverage of joint expertise and experience of two Almac divisions
• Access to both world class technology and drug supply management services
• Reduced vendor management
• Accelerated study start-up
• Rapid adaptation to study
• Improved study communications
• Global capacity

Our Clinical Supply Management offering features the following:

• Lead Almac Contact: A lead Project Manager is allocated to oversee and drive forward the project internally between both disciplines and from an inventory/ drug supply management perspective.

• Shared Master Project Plan: All key deliverable dates are presented in a joint Project Plan, illustrating all milestones for packaging, distribution and the development/ implementation of the IVRS . A clear view of the full distribution process.
• Almac’s standardized drug ordering processes allows for consideration of shipping transit times, import license lead times, depot management requirements and effective management of the kit lists shared between client, distribution and IVRS vendors.

• Integrated reporting: Almac’s integrated web report utilizes data from both clinical trial supply shipping reports and distribution reports from the IVRS. This combined approach permits linkage of IVRS order numbers alongside shipping references and AWB information, providing the full life cycle of drug shipments.  A single unique username and password is provided to users for the integrated web report, the clinical trial supply standard web inventory and distribution reports, as well as standard and customizable IVRS web reports.