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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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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What’s the Difference Between Right to Try and Expanded Access?

The right to try movement and recent passage of the federal right to try law…

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The GDPR and Its Impact on the Clinical Research Community (Including Non-EU Researchers)

The European Union’s General Data Protection Regulation (GDPR) goes into effect May 25, 2018, replacing…

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Integration Update: Recent Milestones Completed

The Advarra team has worked to fully integrate our processes and policies to provide clients…

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Integration Update: Expanded FAQ for Advarra Merger Efforts

The Advarra team (formerly Chesapeake IRB and Schulman IRB) continues to integrate our processes and…

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