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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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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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International Research and Research Ethics Review

Clinical research continues to grow throughout the world, with researchers looking outside the US for…

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Clinical Research Acronyms and Abbreviations You Should Know

New to clinical research? Learn the meaning of common industry acronyms and abbreviations including eCRF,…

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Integration Update: Revised FAQ for Advarra Merger Efforts

Since November 2017, the Advarra team (formerly Chesapeake IRB and Schulman IRB) has been working…

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Data Collection in Clinical Trials: 4 Steps for Creating an SOP

Learn the necessary steps to create an effective SOP for data collection in clinical trials.

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Schulman IRB and Chesapeake IRB Merger and Integration: What You Need to Know

On November 7, 2017, we announced that Chesapeake IRB and Schulman IRB are merging under…

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Changes to NIH Policy for Issuing Certificates of Confidentiality: What You Need to Know

On October 1, 2017, NIH’s policy for certificates of confidentiality (CoCs) changed so that CoCs…

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