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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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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Building Patient-centricity in Clinical Trials: Lessons and Future Directions

  The concept of patient centricity is a recurring theme in clinical research, but the…

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Key CTMS Capabilities to Improve Financial Management

A well-utilized CTMS streamlines financial workflows, automates participant payments, tracks budgets, and centralizes data, helping…

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Why Institutions Should Consider an Externally Administered IBC

Clinical trials for gene therapy are booming, especially in the fields of oncology, infectious diseases,…

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Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)

Read about IND safety reporting required under FDA 21 CFR 312.32(c), challenges faced in adhering…

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Study Activation: Top Four Takeaways from Research Sites

While enrolling subjects is arguably the most crucial aspect of clinical research operations, this cannot…

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