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Harnessing Real-World Evidence and Life Sciences Analytics Transforming Clinical Trials for Enhanced Patient Care

The 7th Annual Real-World Evidence and Life Science Analytics Conference is not just an event; it's an opportunity to be part of the conversation shaping the future of healthcare.<br><br>Become a Sponsor @ https://shorturl.at/0Ttfk<br>

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Harnessing Real-World Evidence and Life Sciences Analytics Transforming Clinical Trials for Enhanced Patient Care

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  1. Real-World Evidence (RWE) and Life Sciences Analytics play crucial roles in modern clinical trials, offering insights beyond traditional clinical trial data. Here's how they're used: Study Design and Protocol Development: RWE helps in designing more efficient and patient-centric clinical trials by providing insights into real-world patient experiences, treatment patterns, and outcomes. This information aids in refining study protocols to make them more reflective of real-world scenarios.

  2. Patient Recruitment and Retention: Life Sciences Analytics can identify potential trial participants from real-world data sources, such as electronic health records (EHRs) and claims data, based on eligibility criteria. This improves patient recruitment rates and ensures the inclusion of a diverse patient population. Additionally, RWE can inform strategies to enhance patient retention by understanding factors that may influence patient adherence and engagement. Control Arm Identification: RWE helps in selecting appropriate control arms for clinical trials by providing insights into the standard of care and real-world treatment outcomes. This ensures that the trial results are compared against relevant benchmarks.

  3. Endpoint Selection and Validation: Life Sciences Analytics aids in identifying relevant clinical endpoints based on real-world evidence of disease progression, patient-reported outcomes, and treatment effectiveness. RWE also contributes to the validation of these endpoints by comparing them with real-world data. Safety Monitoring and Pharmacovigilance: RWE enables continuous safety monitoring throughout the trial and post-market phases by analyzing real-world patient data for adverse events, medication errors, and safety signals. This enhances the detection of potential safety concerns associated with investigational drugs or devices.

  4. Post-Market Surveillance and Labeling: RWE plays a crucial role in post-market surveillance by providing insights into the long-term safety and effectiveness of drugs and medical devices in real-world settings. This information is used to update product labels and inform healthcare decisions. Health Economics and Outcomes Research (HEOR): Life Sciences Analytics contributes to HEOR studies by evaluating the economic and clinical value of interventions in real-world settings. This includes assessing treatment costs, healthcare utilization, patient outcomes, and quality of life.

  5. The 7th Annual Real-World Evidence and Life Science Analytics Conference is not just an event; it's an opportunity to be part of the conversation shaping the future of healthcare. Join us for an inspiring and collaborative experience as we explore ways to bridge insights to impact in the dynamic world of real-world evidence. CONFERENCE REGISTRATION AVAILABLE @ https://shorturl.at/Y8Pwi

  6. Become a Sponsor @ https://shorturl.at/0Ttfk

  7. Become a Speaker @ https://shorturl.at/I2Vel

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