Strategic Expertise to Drive Clinical Success
We craft intelligent, data-driven strategies that set the foundation for clinical trial excellence. By bringing together a multidisciplinary team of experts in medical affairs, operations, regulatory strategy, biometrics, clinical informatics, feasibility, labs, and imaging, we provide a comprehensive approach tailored to your unique development goals.
Our Medical Experts offer deep therapeutic knowledge to refine trial designs and align them with patient needs, while our Regulatory Specialists navigate complex global frameworks to ensure compliance and accelerated approvals. Operational Teams streamline logistics and site management to ensure seamless execution. Meanwhile, Biometrics and Clinical Informatics
harness advanced analytics to deliver real-time insights that inform decision-making and optimize outcomes.
From feasibility assessments to cutting-edge imaging and lab services, our integrated strategy approach transforms complexity into clarity—maximizing efficiency and driving measurable results for every trial.
Partner with iGlobal for precision-driven strategies that bring life-changing therapies to patients faster.
Flawless Execution for Clinical Trial Success
Our approach to Study Execution integrates expertise, technology, and meticulous planning to ensure your clinical trial is executed with precision and efficiency. Every component of trial management—spanning regulatory services to subject engagement—is seamlessly orchestrated to deliver high-quality results while keeping your program on track.
- Regulatory Services & Study Start-Up: Our experts streamline submissions, navigate complex global requirements, and expedite site activations, ensuring a smooth and efficient start to your trial.
- Clinical Trial Management & Vendor Oversight: From managing site performance to coordinating vendors, our operational teams ensure alignment, accountability, and excellence across every touchpoint.
- Subject Recruitment & Retention: Innovative strategies and digital tools enhance enrollment and engagement, minimizing dropouts and maintaining study integrity.
- Safety & Data Integrity: With robust Safety & Pharmacovigilance, Clinical Monitoring, and Data Management, we maintain subject safety and ensure the accuracy of trial outcomes through real-time monitoring and secure data handling.
- Biostatistics & Endpoint Adjudication: Advanced analytics and adjudication services provide clear insights and ensure rigorous scientific standards for endpoint evaluation.
- Comprehensive Quality Assurance: From medical writing to oversight by Independent Data Monitoring Committees (IDMC), every step of our execution framework is supported by best-in-class quality assurance practices.
Our integrated, end-to-end solutions create a cohesive and agile trial management process that adapts to your unique needs. By combining operational excellence with deep therapeutic expertise, we deliver clinical trial execution that exceeds expectations—bringing you closer to approval with efficiency and confidence.
Choose iGlobal Clinical Research to transform your vision into groundbreaking results.
Unified Solutions for Streamlined Clinical Trials
We bring together a powerful suite of integrated services designed to simplify even the most
complex study designs. By consolidating all critical trial functions under one roof, we eliminate
the inefficiencies of working with multiple vendors, enabling you to focus on advancing your
clinical development goals.
- Central & Bioanalytical Labs: Our state-of-the-art laboratories deliver reliable, high-quality data to support every stage of your clinical program, from biomarker analysis to pharmacokinetics.
- Imaging Core Labs: Leveraging cutting-edge imaging technologies and expert interpretation, we provide precise and reproducible data to meet stringent regulatory requirements.
- Cardiovascular Labs: Specialized cardiovascular testing and analysis ensure accuracy in endpoint assessment for trials involving cardiac safety or efficacy.
- Phases I-IV Trials: From early-phase development to large-scale global studies, our integrated model supports seamless transitions between trial phases, maintaining consistency and precision.
Our unified approach ensures all services work in harmony, delivering critical endpoints
efficiently while maintaining the highest standards of quality and compliance. With an
experienced team and robust infrastructure, we provide the expertise and resources needed to
accelerate your trial timelines without compromising results.
Simplify your clinical journey with iGlobal’s Integrated Services—your single solution for
precision-driven research.
Empowering Clinical Research with Advanced Technology
At iGlobal, we leverage cutting-edge technology to simplify processes, enhance decision-making,
and ensure the highest levels of data integrity throughout your clinical trial. Our integrated
suite of tools seamlessly connects every stakeholder, creating a unified platform that delivers
precision, efficiency, and actionable insights.
- Clinical Trial Management System (CTMS): Streamline study oversight with a comprehensive platform that centralizes trial planning, site management, and progress tracking.
- Electronic Data Capture (EDC): Collect and manage data with efficiency and accuracy through intuitive, secure systems designed for real-time reporting.
- ePRO / eCOA / eDiary / eConsent: Engage subjects and streamline trial participation with digital solutions that ensure compliance and enhance the participant experience.
- Interactive Response Technology (IRT): Optimize randomization, drug supply, and logistics with our highly adaptable IRT tools.
- Centralized Monitoring & Imaging Management: Identify risks and trends early with data-driven monitoring solutions, while leveraging advanced imaging tools for precise data analysis.
- iTrial Subject App & iGlobal Site App: Empower participants and streamline site operations with user-friendly, mobile-first applications tailored to enhance trial engagement and compliance.
- Wearables & Lab Information Management System (LIMS): Harness the power of real-time subject data and advanced lab analytics to inform decisions and meet endpoints with precision.
- eTMF (Electronic Trial Master File): Ensure seamless document management with a fully digital, secure system that keeps trial records compliant and accessible.
With our comprehensive technology ecosystem, every phase of your study is seamlessly integrated—connecting
subjects, sites, and sponsors to optimize workflows and accelerate timelines. Our tools are designed to
simplify complexity, provide transparency, and deliver insights that drive successful trial outcomes.
Choose iGlobal’s technology-powered solutions for smarter, faster, and more efficient clinical trials.
