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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Improving Site-Sponsor Relationships Leads to Transparent Clinical Trials

One of the most complicated and multi-faceted relationships in clinical research is the relationship between…

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Patient Engagement and the IRB

Recent years have seen increased efforts to engage with patient and participant communities and include…

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For Sponsors and Sites, the Research Restart Effort Begins With Communication

The global pandemic has changed the way we think about research. Sponsors should consider how…

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Safety Precautions for Laboratory Research With COVID-19 Specimens

The current global pandemic has brought biosafety to the spotlight. Biosafety practices must be customized…

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Trial Design in the Time of COVID-19: Complex and Efficient

Complex trial designs can eliminate less-promising investigational treatments quickly to speed development, but they remain…

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Clinical Trials Day: Thanking the Unsung Heroes

On Clinical Trials Day, now more than ever, it’s important to recognize and thank those…

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Virtual Symposium: Gene Therapy Research in the Age of COVID-19

Gene therapy research continues its rapid expansion in the clinical setting, especially in infectious disease,…

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Generating Leadership Buy-In for a Clinical Research Business Intelligence Solution

As clinical trials increase in complexity, you gain more value from using each resource at…

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Keep in Touch: Tips for Working with a Single IRB for the First Time

Recent regulations and policies have ushered in the era of mandated single IRB (sIRB) review.…

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Q&A – Ask Advarra Live: The Real-World Impact of COVID-19 on Research

Experts from Advarra and Johns Hopkins University School of Medicine provided practical guidance on the…

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Empowering Employees Starts with Building a Strong Culture

Now more than ever, people are seeking out employment at organizations that offer more than…

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Differentiating “Public” and “Private” Internet Spaces in IRB Review

What is the difference between “public” and “private” internet spaces? This question has gained importance…

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