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

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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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Short Form Consents and the Unexpected Non-English Speaking Participant

Short form consents provide a crucial bridge for unexpected non-English speaking participants, ensuring informed consent…

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Beginner’s Guide to eTMF, eISF, and Clinical Research Documents
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Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents

Efficient document systems like eTMF and eISF enhance compliance and streamline document management, helping sites…

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Return of Research Results to Study Participants
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Return of Research Results to Study Participants

Individuals invest a great deal to participate in clinical research, undertaking risks and burdens, while…

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Expanding the Ecosystem to Better Serve You

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Common Pitfalls in Preparing an IND Application

As a drug successfully makes it through the development process, sponsors will inevitably need to…

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The Role of AI in Clinical Research: Opportunities and Ethical Challenges

  Artificial intelligence (AI) is rapidly transforming multiple industries, including clinical research. While AI offers…

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Pharmacovigilance (PV) Organization
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4 Questions to Ask When Establishing a Pharmacovigilance Organization

Establishing a compliant pharmacovigilance (PV) function from scratch is often an overwhelming exercise for emerging…

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A Checklist for Optimizing Clinical Trial Study Startup Activities
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A Checklist for Optimizing Clinical Trial Study Startup Activities

From protocol design to site training, optimizing study startup requires meticulous planning and collaboration to…

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Best Practices in Pre-Screening Includes Use of Technology

Pre-screening subjects is common practice at most sites. In this article, learn some best practices…

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Common Elements of IRB assessments
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Common Elements of IRB Assessments

Like every institutional review board (IRB) – commercial or local – Advarra is subject to…

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Why do Funding and Legal Structure Matter in Decentralized Clinical Trials?

Optimizing clinical trial access for potential patients is a critical goal for researchers and sponsors.…

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Empowering Patients Through Education and Advocacy in Cancer Care

  In the evolving landscape of healthcare, the role of the patient has shifted from…

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