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 Technology and System Integration Can Improve Your Billing Compliance

System integration streamlines clinical trial billing, ensuring accurate charge routing and reducing compliance risks through…

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FDA Inspection Readiness: After the Inspection

In the final part of the three-part FDA inspection readiness series, we will go into…

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FDA Inspection Readiness: During an Inspection

In our previous blog, FDA Inspection Readiness: Preparing for an Inspection we reviewed how to…

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GCP Assessment During COVID – “Did Your Clinical Trials Remain GCP Compliant During COVID-19?”

We are now almost a year into the COVID-19 pandemic, and you may be asking…

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Above & Beyond: Better Utilize In-House Reporting Resources with Advarra Insights

With Advarra Insights’ core dashboards, research institutions streamline reporting, allowing custom teams to target institution-specific…

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4 Reasons Your Institution Needs an eRegulatory System

Finding new ways to more accurately and efficiently manage the regulatory compliance process is always…

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How Sites Can Win in the New Age of Genetically Engineered Treatments

With gene therapy trials on the rise, sites must prepare biosafety protocols, facility standards, and…

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How Staff Augmentation Assists with Successful Data Migration

Staff Augmentation aids data migration by assessing workflows, ensuring a smooth transition to OnCore, and…

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Key Considerations for Regulatory Compliant Document Storage

Compliant document storage in clinical trials demands robust systems for security, accessibility, and retention to…

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Informed Consent: When, Why, and How It’s Obtained

Informed consent isn’t just a formality—it’s an evolving process that safeguards participant autonomy and enhances…

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Q&A: Institutional Responsibilities Under a Federalwide Assurance

In a recent webinar, Advarra regulatory experts presented on the topic titled Institutional Responsibilities Under…

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Understanding the Complexity and Uniqueness of Phase I Trials

In clinical research, working with organizations that understand the ins and outs of the phase…

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