Real-World Data / Real-Word Evidence Resources

  1. Single-Arm Trials Use Real-World Evidence For Rare Disease Drug Development 3/1/2022

    In rare disease product development, where a placebo control group may not be an option, a single-arm trial can be a successful approach. Gain insight into the regulatory considerations for single-arm trials.

  2. How Small And Mid-Sized Biopharmaceutical Companies Can Easily Achieve Digital Innovation For Their Clinical Data 7/12/2022

    Discover how forward- thinking life science companies are defining their vision and looking for like-minded partners to execute information technology.

  3. Leveraging The Window Of Opportunity In Clinical Trial Recruitment 5/13/2023

    Access to real-world data now makes it possible to identify potential trial participants, wherever they are.

  4. Modern Data Platform Strategies That Accelerate Clinical Development 11/26/2025

    A modern data platform is essential for clinical research because it unifies fragmented data, embeds governance, and enables faster, more reliable decision-making.

  5. Trial Tokenization To Understand The Long Term Effectiveness Of A New COVID-19 Vaccine 6/9/2022

    In this case study, learn why a client needed to connect to real world date sources in order to identify potential sources of data that would enable observation of COVID-19 infection rates .

  6. Dysfunctions Of Clinical Trial Vendor Selection And Overcoming Them 10/21/2025

    Vendor selection often fails due to five common dysfunctions. Identifying and addressing them early improves alignment, trust, and trial performance—avoiding costly delays.

  7. How Medidata Link Is Supporting Moderna's Clinical Trial Real-World Data Linkage Initiatives 6/5/2024

    Discover how Medidata Link empowers Moderna's clinical trial RWD linkage initiatives, enhancing insights into treatment outcomes while minimizing administrative burdens.

  8. Reframing Vendor Selection: Beyond Price And Past Relationships 10/21/2025

    An RFP is more than a budget tool — it’s a strategic communication document that guides vendors, clarifies expectations, and enables informed, data-driven sponsor decisions.

  9. Unify Your Data With A Centralized eClinical Platform 3/12/2024

    Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.

  10. Reduce Avoidable Protocol Amendments By Anticipating Operational Pitfalls 5/13/2026

    This report examines how amendment drivers vary across therapeutic areas and how those changes impact execution, patient burden, site workload, timelines, and study costs.