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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Leveraging Data to Lead and Manage the Research Mission

Academic research institutions may not face the financial scrutiny of commercial sites, but they still…

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The Importance of Keeping DSMBs Independent

Establishing DSMB independence helps mitigate bias, ensuring clinical trials adhere to regulatory standards and build…

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Beginner’s Guide to Connected Clinical Research Ecosystems

A well-managed, participant-centric clinical trial has many moving parts, and easy access to the right…

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Beginner’s Guide to Compliant Electronic Source Data Capture

While electronic source data collection is not new, collecting source data in a variety of…

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The Role of Data in Optimizing Clinical Trials: Key Insights for Sites and Sponsors

  In the fast-evolving landscape of clinical research, data collection and performance metrics are indispensable…

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Research Equity and Enrolling Non-English Speakers

Informed consent, a cornerstone of ethical research, involves describing important elements of research in a…

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Understanding International Data Transfer’s Impact

The landscape of data privacy is certainly dynamic and, at times, imposing. In particular, transferring…

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FDA Communications Through the Drug Development Lifecycle

As a drug makes its way through the development lifecycle, one of the most important…

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Data Integrity – It’s All About the Data!

In this increasingly digital world, we have to remember data is now available in many different medians, including paper. When we think…

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6 Tips for Creating Effective Clinical Trial Training

Effective training for clinical trials requires clear, engaging content tailored to busy site staff. Focus…

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Ensuring a Successful and Collaborative SDLC Process

At Advarra, it’s our mission to ensure safer, smarter, faster clinical research every step of…

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4 Questions to Ask CTMS Vendors

Here are four questions to ask during the CTMS selection process to offer more insight…

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