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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Getting “Engaged” in the Time of COVID

When using remote sites to perform clinical trial procedures, there are certain issues researchers must…

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What Do Auditors Look for When Performing SDV and SDR?

Subject safety and reliability of data are paramount in clinical research. This blog outlines what…

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Community Consultation in the Time of COVID-19

How should sites conducting planned emergency research approach community consultation in the time of COVID-19?

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How Oncology Research Is Advancing Better Research

The COVID-19 pandemic has challenged every aspect of the clinical research industry. This new urgency…

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Developing a Clinical Trial Budget Following Medicare’s Clinical Trial Policy and Device Regulations

Developing and negotiating a clinical trial budget that applies Medicare’s rules and regulations involves many…

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IRB Review of Virtual Trial Technologies

Our webinar proved so popular, we thought a deeper dive would be appropriate. In this…

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Q&A – Site and Patient Engagement

CEO Gadi Saarony and Deb Tatton, Parexel Senior Vice President of Global Clinical Operations, consider…

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Q&A – The Evolving Role of Technology

In this Fireside Chat Q&A blog , CEO Gadi Saarony and Deb Tatton, Parexel Senior…

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How Staff Augmentation Services Helps Centralize Site Services

Staff augmentation streamlines research operations, enabling centralized workflows that improve financial accuracy and enhance team…

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Accelerating the Recovery – Design and IRB Review of Safety Monitoring Plans During COVID-19

How do remote visits and data collection impact participant monitoring? What techniques will satisfy the…

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Vendor Qualification vs Requalification Audits: What’s the Difference?

Different types of audits can be performed to support your vendor qualification and management program.…

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The Opioid Crisis in America

The opioid crisis in particular is staggering in the number of lives it has claimed.…

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