Decentralized Clinical Trial Solutions

Accelerating Clinical Development with Tailored DCT Capabilities

At iGlobal, we recognize the increasing demand for flexibility in clinical trial designs. Our Decentralized Clinical Trial (DCT) Solutions provide innovative tools and strategies that empower sponsors, sites, and patients while addressing the unique challenges of today’s clinical research landscape. By blending our proprietary technologies, operational expertise, and global partnerships, we deliver customized DCT models that streamline operations, reduce burdens, and achieve superior results.

Why Choose iGlobal DCT Solutions?

With our tailored decentralized and hybrid trial capabilities, we help sponsors achieve:

  • Faster Patient Recruitment: Reach more diverse populations and accelerate enrollment timelines.
  • Improved Retention: Provide patient-friendly solutions that minimize burdens.
  • Reduced Site and Patient Burden: Seamlessly integrate DCT features to make participation more convenient.
  • Enhanced Data Collection: Real-time visibility into study data improves compliance and operational efficiency.

Nearly all iGlobal studies across therapeutic areas leverage decentralized capabilities to optimize performance, ensuring your trial is positioned for success.

Core Features of iGlobal DCT Solutions

1. Wearable Biosensor Technology

Real-Time Data for Better Insights

Wearable biosensors enable continuous patient monitoring and real-time biomarker data collection. These devices improve trial safety, provide operational efficiencies, and enhance data accuracy.

  • Selection, validation, and logistics for the right sensors.
  • Secure integration of biometric data into trial records.
  • Advanced analysis and visualization tools for regulatory submissions.

2. eConsent

Convenience and Compliance in Informed Consent

Our eConsent solution makes the informed consent process electronic, intuitive, and flexible. Patients can complete the process digitally, improving accuracy and compliance. eConsent forms and data integrate seamlessly into iGlobal’s proprietary iTrack™ Clinical Trial Management System (CTMS), ensuring secure recordkeeping and regulatory compliance.

3. ePRO/eCOA/eDiary

Patient-Driven Data Collection

  • Access data on personal devices via the iEngage™ app.
  • Real-time integration of patient data into the iTrack™ EDC system.
  • Improves subject participation, compliance, and data quality.

4. Direct-to/From-Patient (DtP) Services

Bringing the Trial to the Patient

  • Integrated logistics management via iTrack™ IRT for global shipments.
  • Flexible, country- and site-specific customizations for DtP services.

5. Home Health & Telehealth Services

Convenience for Patients, Efficiency for Trials

  • Reduce enrollment timelines and site visits.
  • Improve retention by increasing convenience for patients.
  • Expand access to diverse populations by removing geographic barriers.

6. Site Solutions

Empowering Sites for Optimal Performance

  • Site Portals: Provide centralized access to study documentation and training materials via iTrack™ CTMS.
  • OnTrack™ App: Supports investigators with real-time study updates, documentation, and protocol access.
  • Recognition Programs: Sites that exceed performance metrics are designated iGlobal Flagship Sites, demonstrating excellence in quality, enrollment, and compliance with DCT strategies.

7. Patient Engagement & Concierge Services

Creating Positive Trial Experiences

  • eRecruitment Tools: Easy-to-use patient platforms for engagement.
  • Concierge Services: Support for travel arrangements, reimbursements, and trial logistics to reduce patient burden.
  • Trial Branding and Advertising: Maximize recruitment success with customized patient outreach campaigns.

8. Centralized Monitoring

Real-Time Oversight and Risk Management

  • Aggregate and review data in real-time across all primary sources, including EDC, IRT, and wearables.
  • Actionable insights allow for proactive decision-making and risk mitigation.
  • Improved operational control and compliance with global regulatory standards.

The iGlobal Advantage in Decentralized Clinical Trials

  • Tailored Trial Design: Customized hybrid and decentralized models to fit your study’s unique needs.
  • Proprietary Technology: Secure and efficient management of decentralized trials through our iConnect™ Platform and its integrated tools.
  • Global Expertise: Leverage our operational experience and partnerships to deliver results on a global scale.
  • Patient-Centric Innovation: Wearables, telehealth, and concierge services improve patient experiences and drive compliance.
  • Data-Driven Decision Making: Centralized monitoring and real-time analytics ensure timely, informed decisions.

Partner with iGlobal Clinical Research to reimagine clinical trial execution with Decentralized Clinical Trial Solutions that deliver results faster, smarter, and with unparalleled precision.