Featured Articles

  1. IBC Vs. IRB: What's The Difference? 7/24/2023

    Learn what separates institutional biosafety committees from institutional review boards and their unique processes for oversight, risk assessments, ethical considerations, and participant risks.

  2. Ace Your Next FDA Inspection 7/24/2023

    This author provides key insights and guidance to sponsors and sites for mitigating risks and ensuring compliance for a successful U.S. Food and Drug Administration inspection.

  3. New & Emerging CMS Policies: Medicaid's New Clinical Trial Policy 7/24/2023

    Explore the key considerations institutions should take into account to best navigate impending CMS changes and what to anticipate for the future of clinical trial enrollment for Medicaid beneficiaries.

  4. Reporting Unexpected Incidents To The IBC 7/24/2023

    Utilize this comprehensive guide to better understand reportable incidents and the appropriate channels for communication when unforeseen events arise.

  5. Perceptions Of Clinical Trials 7/24/2023

    Dive into the poll results from 1,000 random U.S. residents for an overview of their general perception and understanding of clinical research.

  6. Data Safety Monitoring Boards Facilitate Ethical Research 7/19/2023

    Unearth how DSMBs ensure the protection and safety of trial participants and the integrity of scientific data by monitoring trial results.

  7. Phases Of Clinical Research: A Detailed Overview 7/19/2023

    Delve into the protective measures implemented during each clinical research phase to safeguard study volunteers from potential harm and ensure the effective development of new drugs and therapies.

  8. NCI-Designated Hospital System Trains 400 Users, Enhancing Efficiency & Consistency 5/17/2023

    Explore how a large National Cancer Institute (NCI)-designated hospital system was able to train its teams remotely—and at their own individual pace—to fulfill organizational goals.

  9. Research Site Network Enhances Study Startup With Reliable ICF Writing Services 5/17/2023

    With help from a new informed consent form (ICF) writing partner, discover how CenExel Clinical Research was able to streamline processes and launch new studies faster.

  10. Top Biopharma Enhances Regulatory Efficiency 5/17/2023

    Learn how this biopharma company was able to assemble project teams focused on implementing real-time document transfer for central IRB documentation and communications, significantly reducing errors and improving data management.