Webinars

  1. Navigating Diverse Reporting Requirements In Pharmacovigilance 5/30/2023

    Explore various regional approaches for implementing E2B(R3) and IDMP, the challenges often faced in producing a single ICSR, and the advancements in electronic ICSR reporting and their impact on compliance.

  2. Automating Study Setup With A Digital Data Flow 5/30/2023

    Using the efforts of TransCelerate Biopharma, working with Accenture, as an example, see how teams were able to automate study setup by developing the tools and processes to support upstream systems like study builder and protocol authoring tools.

  3. Creating The Future In Clinical Research With CROs Using RWD 5/30/2023

    Explore the many ways that real-world data (RWD) is gaining significance in clinical research and healthcare decision-making processes.

  4. Do DCTs Offer Clinical Precision In Challenging Patient Populations? 5/30/2023

    Examine the evolving guidance from regulatory agencies regarding decentralized trials and its impact on the role and responsibility of sites when working with challenging populations, in addition to practical methods for ensuring effective patient oversight and data monitoring.

  5. Accelerating Adoption & Lowering TCO With An RTSM System 5/30/2023

    Gain insight from industry experts on new discoveries in cancer therapy, how data is being used to drive organizational decision-making, RTSM systems in clinical trial operations, and their solutions for standardization.

  6. The Conundrum Of Proliferating Data From Decentralized Clinical Trials 5/30/2023

    The advent of decentralized clinical trials has opened a unique opportunity to gain unprecedented insights into patients' study experiences. Watch speakers answer the industry’s tough questions about hybrid trial designs, streamlining workflows, adopting data capture methods, and more.

  7. Driving Success & Transformational Initiatives In Clinical Trials 5/30/2023

    Realize the value of investments in clinical research and pharmacovigilance operations through business assessments, best practices, enablement, mentoring, industry peer interaction, and professional services.

  8. How CROs Are Leveraging Innovation To Accelerate Clinical Trials 5/30/2023

    Learn how CROs advance clinical trials by adopting innovations, impactful technologies, and operational shifts, and how modern trial designs can be offered at scale today.

  9. Advanced Methodologies For Signal Detection In Emergency-Use Cases 5/30/2023

    Dive into the relationship between target products and adverse events, the potential of masking and confounding these relationships, and what new results are showing the industry today.

  10. How EU 536/2014 Will Revolutionize Global Clinical Trials 5/30/2023

    Don’t miss this conversation where speakers explore the requirements for global submission oversight and avoiding global study time penalties, critical global business roles to manage successful EU submissions, new system features needed to attain successful EU submissions, and details on why EU 536/2014 will require coordinated, detailed global and EMEA planning and management.