Real-World Data / Real-Word Evidence Resources

  1. Could ePRO Be The New Standard In Health Reimbursement? 1/30/2023

    Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.

  2. Patient Diversity Case Study: RWD Solutions 7/18/2022

    See how by leveraging medical claims and diversity data, this clinical trial sponsor was able to identify relevant patients meeting the trial’s I/E criteria, broken out by race and gender.

  3. How Can Real-World Data Benefit Your Trials? 3/12/2024

    Clinical trial data is being supplemented with real-world data (RWD) gathered from a variety of sources. Dive deeper into this emerging trend to understand its implications for the future of clinical research.

  4. Real-World Evidence - Where Are We Now? 8/24/2022

    Notwithstanding ongoing confusion over the concepts of “real-world data” and “real-world evidence” in 2022, more than 5 years after the passage of the 21st Century Cures Act, the FDA continues to evaluate such data and evidence as it considers regulatory decisions.

  5. The EMR Interoperability Dream Vs. Clinical Research Reality 10/20/2025

    Seamless Electronic Medical Record access promises accelerated trials and regulatory-grade evidence, but incomplete, unstructured data requires hybrid strategies using AI and human oversight to bridge gaps.

  6. Navigating Biases In Clinical Trial Vendor Selection 10/21/2025

    Biases, often hidden, can distort vendor selection decisions. Recognizing and addressing them across individuals and teams leads to more objective, aligned, and successful clinical trial outcomes.

  7. Harnessing The Power of Real-World Data In Clinical Trial Planning 2/20/2024

    As the availability of RWD grows, it creates opportunities for sponsors to use true patient insights to support their clinical strategy and bring treatments to patients in need.

  8. Expedite Drug Development With An Integrated CDMO-CRO Model 2/6/2026

    From optimizing first-in-human strategies to leveraging AI-enabled digital architectures, the integrated CDMO-CRO services model reduces risk and maximizes program value.

  9. Optimize Your Oncology Trial Protocol With Real-World Data 9/16/2024

    Set your next oncological clinical trials up for success using high-quality real-world data (RWD) to anticipate and confront potential problems early on.

  10. Overcoming Issues Of Non-Enrolling Sites In Clinical Trials 1/14/2025

    Explore the challenges of non-enrolling sites in clinical trials, focusing on the benefits of leveraging artificial intelligence (AI) and machine learning (ML) in addressing those issues.