WE HARNESS THE POWER OF DECENTRALIZED CLINICAL TRIALS

OUR TAILORED DCT SOLUTIONS OFFER UNRIVALED EFFICIENCY, UNPARALLELED DATA ACCURACY, AND AN UNWAVERING COMMITMENT TO PUTTING PATIENTS FIRST

Why Work with Us

Benefits of DCT
  1. Streamlined Efficiency:
    Reduce site visits by up to 40% and slash administrative burdens, allowing your team to focus on critical tasks.
  2. Enhanced Data Accuracy:
    Real-time data collection and remote monitoring significantly reduce data entry errors, with accuracy rates exceeding 95%.
  3. Patient-Centric Approach:
    Empower participants with remote visits and flexible scheduling, resulting in 30% higher recruitment rates and increased participant satisfaction.
Best Practices
  1. Cutting-Edge Technology:
    Leverage state-of-the-art digital infrastructure and secure platforms for seamless remote data collection and analysis.
  2. Remote Engagement:
    Engage participants through remote monitoring, virtual visits, and home-based sample collection, enhancing convenience and accessibility.
  3. Data Security and Privacy:
    Implement stringent measures to protect participant privacy and comply with regulatory requirements, ensuring data integrity.
Advantages for Biotechs and Trial Sites
  1. Increased Efficiency:
    Reduce site workload, minimize source data verification, and accelerate trial timelines, leading to up to 30% faster study completion.
  2. Improved Data Quality:
    Real-time data monitoring and centralized review enable early detection of safety concerns and insights for optimized decision-making.
  3. Patient Satisfaction:
    Eliminate travel burdens and offer flexible participation options, resulting in 20% higher participant engagement and retention.
When DCT May Not Be Suitable
  1. Complex Procedures:
    Trials involving intricate interventions may require a hybrid approach, combining remote and site-based assessments.
  2. Limited Technology Access:
    Evaluate participant access to technology and internet connectivity to ensure seamless participation, considering target demographics.
Alternatives
  1. Hybrid Trials:
    Optimize efficiency by combining remote and site-based visits, maintaining essential in-person assessments while reducing overall burden.
  2. Siteless Trials:
    Conduct trials entirely in a remote setting, leveraging digital recruitment and decentralized data collection for maximum convenience.
  3. Virtual Site Models:
    Establish virtual research sites, engaging investigators and participants remotely, minimizing physical visits and costs.
Success Strategies
  1. Collaborative Partnerships:
    Foster strong relationships with trial sites, providing comprehensive training and support to ensure successful DCT implementation.
  2. Regulatory Compliance:
    Stay up-to-date with regulations, obtain necessary approvals, and safeguard participant data to maintain regulatory compliance.
  3. Ongoing Evaluation:
    Continuously assess and adapt DCT processes based on participant and investigator feedback, ensuring optimal performance and participant satisfaction.