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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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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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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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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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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Building Customer Experiences That Lead to More Hope for Patients

Clinical research gives people hope. For some, it’s the chance to hold a new grandchild.…

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Clinical Trial Budget Negotiations: A View From Each Side

Budget negotiation success hinges on clear communication and early resource sharing, helping sites and sponsors…

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