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Edwards Life Sciences

How Edwards Life Sciences Increased Site Efficiency by 40% and Reduced Risks by 25% in Eight Months

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Challenges

Monitoring and Managing Metrics

ELS needed to understand and elevate performance metrics across diverse clinical sites and studies.

Streamlining Clinical Affairs

The manual reporting processes required automation, and the Clinical Affairs team needed user-friendly analytics dashboards.

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Improving Site Selection and Negotiation

Data was crucial for optimizing site selection and monitoring contracts efficiently.

Enhancing Enrollment Metrics

High enrollment rates needed tracking, and high-risk sites required proactive mitigation.

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Solutions

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  • Comprehensive Data Audit and Analysis

    Conducted thorough data audits and implemented advanced analytics to improve site performance metrics.

  • Power BI Dashboard Design

    Designed intuitive dashboards for real-time monitoring, enabling swift and informed decision-making.

  • Strategic Business Intelligence Consulting

    Aligned ELS’s operational goals with data strategies through expert consulting.

  • Team Training and Support

    Delivered training to maximize system utilization and adoption of new tools.

Process

The company faced numerous challenges in implementing new solutions. We decided to utilize modern approaches and tools to achieve maximum efficiency.

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  • 01 Discover

    In the first phase, we conducted a detailed analysis of existing processes and identified key requirements for the future project.

  • 02 Design

    The second phase involved designing solutions tailored to user needs and business objectives, ensuring intuitive interfaces.

  • 03 Develop

    The third phase encompassed the actual development and implementation of new solutions using advanced technologies.

Results

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  • Enhanced Site Performance Monitoring

    Increased efficiency in monitoring and managing clinical site performance by 40%.

  • Automated Reporting Efficiency

    Reduced manual reporting time by 50%, improving efficiency for tracking Protocol Deviations and Adverse Events.

  • Accelerated Decision-Making

    Improved decision-making speed in clinical affairs by 35%.

  • Optimized Site Selection

    Enhanced site selection efficiency by 30% and reduced contract negotiation time by 20%.

  • Improved Enrollment Metrics

    Achieved a 15% increase in enrollment efficiency across studies.

  • Reduced Clinical Trial Risks

    Decreased adverse event incidents by 25%.

     

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