Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

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Ways to Streamline Informed Consent Process in Clinical Trial Startup

Optimizing the informed consent process is critical for accelerating clinical trial startup while maintaining compliance and participant understanding. This article explores key strategies for streamlining informed consent, including leveraging electronic consent (eConsent) solutions, standardizing templates, and improving collaboration between sponsors, sites, and IRBs. By implementing these best practices, research teams can enhance efficiency, reduce delays, and improve the participant experience in clinical trials.

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Beginner’s Guide to Minimal Risk Research

When an institutional review board (IRB) determines research is “minimal risk” (as defined in Department…

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Beginner’s Guide to Independent Asset Reviews

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Understanding Medical Science Liaisons and Clinical Liaisons

Research organizations utilize a variety of medical professionals to conduct successful clinical trials. Two of…

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Different Players Involved in Reviewing Clinical Research

  Clinical trials play a critical role in the development of new drugs and devices,…

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Maintaining a Robust Clinical Trial Pipeline

The clinical research landscape is likely forever altered by the COVID-19 pandemic, especially regarding trial…

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4 Key Integrations for Your Clinical Trial Management System

In this blog are some key CTMS integrations — using systems your institution has likely…

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Why it is Critical to Have and Enforce a Data Strategy?

The Call to Action Data is the most important asset for a pharmaceutical or biotechnology…

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Optimizing a Clinical Development Program to Improve ROI

Clinical development proceeds in phases, and each phase contains a set of clinical trials. These…

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IRB Review of Social Media Recruitment and Retention Programs

Social media can be a valuable tool for researchers to connect with and recruit potential clinical…

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The Value of Early Engagement with Your IRB

It’s no secret that in clinical research, everything moves at a quick pace – and…

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Ideas for Managing Clinical Trial Finances Post-Pandemic

While the pandemic’s long-lasting effects on clinical trials are not yet fully known, effective financial…

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How to Design Digital Materials for Participant Engagement

Informative and engaging participant materials are an important part of any clinical trial, especially during…

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