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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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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Making a Case for Interim HRPP Staffing

As much as we hate to admit it, many of us have been there…that moment…

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Coverage Analysis: Standard of Care vs. What Medicare Covers

A thorough coverage analysis identifies billable items in clinical trials, balancing standard of care needs…

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Fitting Your Needs: Pandemic-Proofing Protocols

With more than half of 2020 underway, it’s safe to say the year is not…

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Introducing Fireside Chats: Conversations On Burning Research Topics

Advarra is excited to introduce Fireside Chats, a series of virtual conversations discussing current issues…

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Q&A – The New Normal: Considerations for Restarting Research

In a recent webinar, Advarra IRB and research compliance experts discussed key areas to consider…

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7 Staff Augmentation Resources to Help Your Site Restart Research

You likely have short-term projects to be completed quickly, or large ongoing projects delayed due…

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Q&A Part 1 – Gene Therapy Research in the Age of COVID-19

In Advarra’s inaugural virtual symposium, experts from industry and academia met to discuss the unique…

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Q&A Part 2 – Gene Therapy Research in the Age of COVID-19

In Advarra’s inaugural virtual symposium, industry and academic experts discussed overcoming obstacles and optimizing study…

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