Featured Articles

  1. IRB Review Of Changes To Previously Approved Research 5/15/2024

    Learn why understanding the intricacies of IRB review for study changes is essential for researchers and institutions, covering everything from minor amendments to significant modifications.

  2. CRO Leverages Integrated Central IBC Partnership To Initiate Sites 5/15/2024

    Learn how a CRO was able to accelerate review times so COVID-19 vaccine trial sites could progress through site selection, IRB/IBC submission, approval, drug shipment, and complete site initiation visits in record time.

  3. Reinvigorating Your Human Research Protections Program 5/15/2024

    By bringing objective evaluation, expertise, and effective change management skills, learn how interim staff can improve an institution’s ability to identify issues and implement necessary changes.

  4. Planning For Complex Change At Your Organization 5/15/2024

    With technology advancing clinical operations, proactive adaptation is paramount for organizations to remain at the forefront. How can your organization effectively navigate these evolving dynamics?

  5. Key Items Auditors Look For When Reviewing An Investigator Site File 5/15/2024

    Gain insight on how to prepare investigator site files (ISF) for audits and what teams should consider when looking to enhance efficiency and compliance.

  6. Strategic Training: Navigating Organizational Challenges 5/15/2024

    While training is beneficial, it's not universally required. The crucial aspect lies in ensuring that stakeholders understand the purpose of the training and whether it's the most effective solution.

  7. Top 20 Pharma Accelerates Training And Enrollment Across 650 Site Staff 5/14/2024

    With Longboat, this pharma company trained all staff across trial sites, ensuring treatment for all 20,000 patients with real-time training reports.

  8. Top Biotech Achieves Recruitment And Improves Compliance Across 30 Sites 5/14/2024

    Uncover how a biotechnology company experienced recruitment and compliance success after utilizing Longboat to provide training for every staff member at every trial site.

  9. Reporting To The IRB: Investigator Noncompliance 4/19/2024

    Reporting noncompliance concerns is crucial to protect research participants, allowing researchers can ensure ethical research conduct and protect the rights and welfare of participants.

  10. Understanding FDA's 2024 Draft Guidance On DMCs 4/19/2024

    By integrating independent Data Monitoring Committees into trial management processes, learn how sponsors can enhance trust, integrity, and the success of their clinical trials.