Didn’t Expect That to Happen: Events That Must be Reported Promptly to the IRB
Learn what events need to be reported to the IRB after study approval and explore scenarios to help evaluate potentially reportable events.
Learn what events need to be reported to the IRB after study approval and explore scenarios to help evaluate potentially reportable events.
Switching from paper to eSource in clinical trials enhances data accuracy, reduces errors, and boosts organization, offering more efficient study management.
Decentralized clinical trials (DCTs) are transforming clinical research by allowing data collection from participants outside traditional settings, such as
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
In the evolving landscape of clinical research, increasing diversity, equity, and access has become a pressing priority. A Clinical
Key ROI metrics—like publications, staff impact, and core contributions—provide insight into research value and support institutional growth.
In the fast-evolving landscape of clinical research, data collection and performance metrics are indispensable tools for enhancing the efficiency
Clinical trials play a critical role in the development of new drugs and devices, ensuring they are both safe
Diversity and Inclusion: Who is Responsible – Site, CRO or Sponsor? Attaining a diverse trial patient population is crucial to
The concept of patient centricity is a recurring theme in clinical research, but the industry has only just begun
Clinical trial activation involves a host of tasks, from institutional review board (IRB) tasks and consent form development to
Gene therapy is rapidly transforming from an experimental treatment into a cornerstone of modern medicine. Once confined to major