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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Why Device, Diagnostic, and Digital Therapeutic Research Needs Endpoint Adjudication

In its March 2006 guidance, Establishment and Operations of Clinical Trial Data Monitoring Committees, the…

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Understanding the EU Clinical Trials Regulations Updates

The updated European Union (EU) pharmaceutical legislation for the Clinical Trials Regulation (CTR) entered into…

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Improving Regulatory Workflows in Study Startup

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Addressing Research Technology Challenges to Gain Sponsor Buy-in

At Advarra, we are passionate about enabling the industry to become more site-centric. To achieve…

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Considerations for IRB Review: Artificial Intelligence & Machine Learning

Artificial intelligence in clinical research is expanding rapidly, bringing both excitement and ethical challenges. How…

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DMC vs EAC: What’s the Difference?

Clinical research oversight relies on both DMCs for big-picture data review and EACs for detailed…

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Beginner’s Guide to Clinical Trial Billing Compliance

Understanding clinical trial billing rules, from Medicare policies to state laws, is crucial for avoiding…

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Local Versus Central IRBs: What’s the Difference?

Central and local IRBs share the same research oversight goals, but NIH’s single IRB mandate…

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Advarra’s Support for Institutions

As clinical research sites face more challenges than perhaps ever before, it’s increasingly important to…

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Beginner’s Guide to institutional review boards (IRBs)

In clinical research, institutional review boards (IRBs) a vital role in ensuring participant rights and…

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eClinical Regulatory Trends Impacting Clinical Research

For the past two years, the clinical research industry has seen an acceleration in staff…

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Keys to Advancing Your Biotech Go-to-Market Plan

For nearly 10 years, a growing biotech company worked to develop a nitric oxide and…

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