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Articles Tagged With: irbs

  • Chief Ethical Considerations for Continued COVID-19 Vaccine Research

    The COVID-19 pandemic has created more uncertainty in human research protections in 2021. One issue IRBs will face is whether the benefits continue to outweigh the risks for people who enroll in COVID-19 vaccine studies.

  • 20 Years of Reports on Research Protection

    To commemorate the past 20 years of human research protection, as well as two decades of IRB Advisor, we asked editorial advisory board members to comment on how things have changed since 2001.

  • IRB Websites Can Offer a Wealth of Useful Tools

    An important and useful function of an IRB’s website is its ability to give researchers — as well as the public — access to a wide variety of forms, guidance, and tools. When created well, an IRB’s website can be easy to navigate. It also should be updated with new and revised information regularly. Like crowdsourcing websites and with permission, an IRB’s website also can adopt and adapt tools that researchers and other IRBs have found useful.

  • Investigators Benefit from Using Online Self-Auditing Tools

    One method to improve regulatory compliance while maintaining IRB efficiency lies in teaching investigators how to conduct self-audits of their protocols and studies.

  • Self-Assessing IRB Operations Can Help HRPPs Stay Compliant, on Track

    If an IRB sets a goal of greater efficiency, then giving researchers self-assessment tools and using self-auditing tools on IRB operations is a method that can work. These tools can help study coordinators and investigators turn their study protocol submissions from a hot mess into a submission that is mostly compliant and easier to pre-review.

  • Government Accountability Office to Study For-Profit IRBs at Senators’ Request

    The Government Accountability Office agreed to “investigate the operations” of commercial IRBs at the request of U.S. Sens. Elizabeth Warren, D-MA, Sherrod Brown, D-OH, and Bernie Sanders, I-VT.

  • Research Professionals Question Structure, Effectiveness of IRBs

    Finding ways to evaluate IRB ethical quality and effectiveness has been an elusive ideal. Two research professionals are advocating for directly measuring quality of board oversight, rather than relying on the structure of the IRB. An upcoming U.S. Government Accountability Office evaluation of commercial IRBs also may promote the conversation.

  • Tips to Improve IRB-Researcher Productivity and Relationship

    Expectations and communication issues are the two biggest challenges between principal investigators and the IRB community. IRBs set expectations through their websites and response letters, but they might not have articulated those expectations to themselves and investigators. From the principal investigator perspective, researchers might not fully appreciate that IRBs can be advocates and not merely a clearing house or impediment to putting research in the field.

  • Tips for Reopening or Closing Research Studies

    The 2020 landscape for clinical trials looks different than it did five or 10 years ago. Even before the worldwide disruption in research from the COVID-19 pandemic, there were systemic shifts that have squeezed trials in ways that add pressure to investigators and IRBs.

  • IRBs Look at How to Get Through Pandemic — and Beyond

    As human research protection programs and IRBs enter the next leg of the COVID-19 pandemic, they can draw on experience to find the best balance between safety and efficiency. Each institution and IRB will face its own challenges. But one of the more common challenges as the United States copes with more than eight months of the crisis is pandemic fatigue and burnout.