Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

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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Tips for Writing Effective Edit Checks in eCRFs

Edit checks are a great mechanism to improve data quality within an electronic data capture…

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Q&A – Study Startup Success for the New Generation of Genetically Engineered Vaccines

In a recent webinar, Advarra Executive Director of Biosafety Services Daniel Eisenman discussed the latest…

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Beginner’s Guide to Investigator-Initiated Trials

While many clinical trials are initiated by industry sponsors, such as pharmaceutical companies or contract…

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5 Tips for Successful Project Management in Clinical Research

Project management is a key part of every successful business, and the clinical research industry…

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Is GDPR Coming to the US? CCPA and Its Impact on Research

Remember on the older The Price Is Right game shows with Bob Barker, when the…

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Q&A – The Must-Haves of FDA and Common Rule Reporting Requirements

In a recent webinar, Advarra regulatory experts discussed the must-haves of FDA and Common Rule…

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2020 Fall Onsemble Conference
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Onsemble: Fostering Collaboration and Community

At Advarra, we are passionate about empowering our customers to advance better research. Last year,…

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Beginner’s Guide to Continuing Education Units (CEUs) for Clinical Research

Many organizations require their employees to complete continuing education requirements in order to stay current…

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3 Essential Elements of Change Management Within Clinical Research Operations At Your Research Site

The key to effective, productive change within a research institution lies at the nexus of people,…

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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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