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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Community-Based Participatory Research (CBPR): A Framework for Community Engagement

Community-based participatory research (CBPR) continues to come up in conversations surrounding diversity and inclusion in…

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Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials

The data gathered in a clinical trial is often collected by many different people, including…

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The Many Faces of “Coercion” and “Undue Influence”

The United States regulations governing research with humans pay special attention to two ethical concepts…

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Coming Together to Benefit the Greater Research Community

At Advarra, our mission is to advance human health by empowering compliant, efficient, and collaborative…

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Q&A – Racial Diversity in Clinical Trials: Building Trust in Participant Engagement

In our latest webinar, a panel of experts from research organizations, Community Health Centers (CHCs)…

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Surprise! “Checking the Box” Is Still an Option on the Federalwide Assurance (FWA)

The Common Rule (subpart A of 45 CFR part 46) requires that each institution engaged…

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Takeaways From the FDA’s VRBPAC Meeting – October 22, 2020

As part of FDA’s response to combat COVID-19, FDA convened its Vaccines and Related Biological…

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Tips for Writing Effective Edit Checks in eCRFs

Edit checks are a great mechanism to improve data quality within an electronic data capture…

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Q&A – Study Startup Success for the New Generation of Genetically Engineered Vaccines

In a recent webinar, Advarra Executive Director of Biosafety Services Daniel Eisenman discussed the latest…

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Beginner’s Guide to Investigator-Initiated Trials

While many clinical trials are initiated by industry sponsors, such as pharmaceutical companies or contract…

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5 Tips for Successful Project Management in Clinical Research

Project management is a key part of every successful business, and the clinical research industry…

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Is GDPR Coming to the US? CCPA and Its Impact on Research

Remember on the older The Price Is Right game shows with Bob Barker, when the…

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