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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Navigating the FDA Emergency Use Filing Process

In an effort to create safe, effective, and affordable ventilators to help combat the foreseeable…

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Developing an Emergency Preparedness Plan for your HRPP

The COVID-19 pandemic highlighted the importance of robust emergency preparedness for HRPPs, ensuring research continuity…

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Considerations for Transitioning from Paper to eSource

Switching from paper to eSource in clinical trials enhances data accuracy, reduces errors, and boosts…

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The Evolution of IRB Reviews in Decentralized Clinical Trials

  Decentralized clinical trials (DCTs) are transforming clinical research by allowing data collection from participants…

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Improving Patient Centricity and Research Access

A clinical research trial can only be as strong its participant population, but it’s challenging…

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For FDA Inspection Readiness, Accountability is Key

Dawn Wydner, former Food and Drug Administration (FDA) Consumer Safety Officer, LCDR, and current Managing…

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Top 10 Educational Resources of 2021

The year 2021 brought many advancements in the clinical research industry. We’ve pushed for more…

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Q&A: FDA Updates: BIMO – What Sponsors Need to Know

Advarra experts Joan Versaggi and Leslie Paul answer questions from the first in the webinar…

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The Key to Increasing Diversity in Decentralized Trials

Historically, decentralized clinical trials (DCTs) were heralded as the future of patient-centered research. But how…

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Unique Ethical Issues in Phase I Oncology Studies

Phase I oncology trials present distinct ethical challenges, such as participant vulnerability and the risk…

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Returning to In-person Work: Sponsor Versus Site Viewpoints

As March 2020 completely disrupted any sense of normalcy, including in the workplace, many were…

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Increasing Diversity, Equity, and Access in Clinical Research: A Case Study

  In the evolving landscape of clinical research, increasing diversity, equity, and access has become…

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