Advarra Blog

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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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IRB Review of Phase I Research: Balancing Ethics and Efficiency

Phase I research demands careful IRB oversight, balancing participant safety with timely reviews. Proactive strategies…

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3 Must-Haves to Deploy Remote Clinical Trials

This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities…

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Understanding eSource, ePRO, and EDC

eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant…

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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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