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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Meeting the Challenges of Investigator-Initiated Trials

Stem cell clinics with unproven treatments are on the rise in the US. Learn how…

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The Challenge of Unproven Regenerative Stem Cell Therapies

Stem cell clinics with unproven treatments are on the rise in the US. Learn how…

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Survey Best Practices for Process Improvement

Before diving into your survey, brush up on the basics and best practices of survey…

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Six Key GDPR Questions to Review

Questions still remain about GDPR and its applications. Have you considered these six key questions…

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Can Ethics Review Catch Up to the CBD Craze?

CBD, a non-psychoactive cannabinoid, is experiencing a massive surge in popularity, but clinical research lags…

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Quorum/Kinetiq Acquisition & Integration:<br>What You Need to Know

On March 5, 2019, Advarra announced its acquisition of Quorum Review IRB and Kinetiq, the…

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After the Compliance Date: Revised Common Rule FAQs (Or: Why We Cancelled Our February Webinar)

The bad news is we cancelled our webinar on the revised Common Rule. The good…

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Informed Consent Changes in the Revised Common Rule

Many of the revised Common Rule’s changes aim to make informed consent more meaningful, so…

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Do I Need to Comply With the Revised Common Rule?

Most requirements of the revised Common Rule go into effect January 21, 2019*. While many…

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Infection Control and Biosafety in Gene Therapy Research

Gene therapy research has moved from the realm of science fiction to mainstream clinical research.…

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Integration Update: Leading Compliance Adherence

The Advarra team is proud to announce that all major integration activities are now complete.…

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ICH-GCP Guidelines and Research Conducted in the US

When research is being conducted in multiple countries, determining which regulations apply to which country’s…

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