Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

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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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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IRB Review of Phase I Research: Balancing Ethics and Efficiency

Phase I research demands careful IRB oversight, balancing participant safety with timely reviews. Proactive strategies…

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3 Must-Haves to Deploy Remote Clinical Trials

This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities…

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Understanding eSource, ePRO, and EDC

eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant…

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Beginner’s Guide to Minimal Risk Research

When an institutional review board (IRB) determines research is “minimal risk” (as defined in Department…

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