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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Francine Lopez Senior Manager Client Services Advarra
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Q&A with Senior Manager of Client Services Francine Lopez

For nearly a decade, Francine Lopez has helped clinical research move from idea to impact.…

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Rethinking Oncology Trial Design: Turning Insights from Data and Experience into More Feasible Studies

Oncology research continues to push scientific boundaries, from biomarker-driven therapies to increasingly personalized treatment strategies.…

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Insights on the FDA’s ELSA AI And What Changes Next 

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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Preparing for Elsa: What Sponsors, Sites, and CROs Need to Know About the FDA’s New AI Era 

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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Doctor wearing gloves writes on paper beside a keyboard in an office setting.
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Simplifying Oversight and Managing Regulatory Complexity in Multi-Site Clinical Trials 

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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Q&A with Advarra’s Client Experience Team Lead Jennifer DeZurik

Client Experience Team Lead Jennifer DeZurik brings both professional and deeply personal connections to Advarra…

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 How to Select a Clinical Trial Management System 

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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Integrating AI to Balance Scientific Rigor and Real-World Feasibility in Clinical Trial Study Design  

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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How Sponsors Can Use Adaptive and Platform Trial Models to Reduce Amendments and Accelerate Study Start-Up 

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive…

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Q&A with Advarra’s Client Experience Partner Brian Boggs

As a member of Advarra’s client experience team, Brian Boggs plays a pivotal role in…

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Enabling Oncology Site Success: Tackling the Barriers That Slow Cancer Research

Oncology clinical trials are becoming increasingly complex, placing new operational and administrative demands on both…

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Anna Carnevale Advarra
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Q&A with Advarra’s Associate Director of Client Services Anna Carnevale

Over the past 14 years, Anna Carnevale, associate director of client services at Advarra, has…

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