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 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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Effectively Working with a Research Technology Vendor During Implementation

As a research site starts the adoption and implementation process for a new technology, there…

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Advarra Trend Report: Analyzing Sites by Organization Type

Since early 2020, clinical research sites – like many industries – experienced profound COVID-19 impacts.…

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Maintaining Data & Reporting Integrity with Mobile Health

As the COVID-19 pandemic has forced a shift toward remote modalities, mobile health (mHealth) technologies…

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Op-ed: Missing Elements of the Discussion on Decentralized Trials

The discussion on decentralized clinical trials (DCTs) has been brought to the forefront in the…

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Does This Study Require IBC Review?

Gene therapy research is highly regulated due to associated risks, often leading to confusion among…

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4 Questions to Ask When Evaluating Your Research ROI

Key ROI metrics—like publications, staff impact, and core contributions—provide insight into research value and support…

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Sites: The Key to Patient Centricity in Clinical Research

We’ve heard and used the term “patient centricity” for years now, and with good reason.…

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Connecting Patient Centricity and eConsent Together

Patient-centric trial design, combined with eConsent, fosters better communication, comprehension, and retention, ensuring a smoother,…

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