Clinical Trial Management

Cenduit’s Interactive Response Technology (IRT) is not just about “technology”.  It’s about clinical study solutions that focus on transforming data-driven decision making throughout the drug development process. Cenduit’s consultative approach and innovative portfolio of products and services allow us to connect sponsors, investigator sites, clinical trial suppliers and clinical research organizations ― with measurable efficiencies.

Program Management

• Site selection: Typically 30% of sites never recruit a single patient
• Most common indications have more than 5 concurrent projects running in EU and US
• Estimated 25% typical wastage on the clinical side of program management

Site/Patient Management

• Inclusion/Exclusion criteria enforceability
• Uniform site communication
• Streamlined eDiary setup/assignment for sites and patients
• Timing of CRA visits synchronized with patient enrollment
• Deliver right drug to right patient at right time
• Controlled un-blinding process
• Electronic audit trail of drug dispensation

Data Management

• IRT is the first point of entry for patient data
• Patient data is entered in four or more places by four different layers of personnel handling a trial
• Significant reduction in ePRO data queries by eliminating redundant data entry
• Duplication of data queries estimated to be in the region of 25% in trials without a “single source of truth”

Supplies Management

• Typical overage in clinical trials can exceed 200%
• Huge regulatory impact of expiry date inaccuracy
• Integrated inventory management for device-based patient eDiaries
• Sophisticated algorithms are required to configure supplies management and require supply chain core competence in IRT personnel

Are you ready to learn more? Do you have a question on how we can help you with Clinical Trial Management? Please contact our team via the form below.