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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Q&A – The New Urgency of Clinical Trials: How Oncology Leads the Evolution

In Advarra’s recent virtual symposium, experts from industry and academia met to discuss how oncology…

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Improve Data Quality With 5 Fundamentals of Clinical Data Management

Gathering high-quality, reliable and statistically sound data is the goal for every clinical trial; and…

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Roles and Responsibilities of a Clinical Research Coordinator

In clinical research, it’s no secret that clinical research coordinators (CRCs) are tasked with an…

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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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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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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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