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Efficient Clinical Trials

Latest Efficient Clinical Trials Resources

Virtual Trials and the Site’s Role in a Shifting Research Landscape

Virtual trials have grown in popularity and usage over the last decade. Explore what that means for traditional sites and their future in the clinical research landscape.

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4 Valuable Integrations for Your Clinical Trial Management System

Implementing and integrating a CTMS can be beneficial for your organization. Streamline your research operations with these 4 integrations.

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Understanding the Types of FDA Inspections

Receiving notice of an FDA audit can be stressful for an organization. Breaking down the different types of inspections, here’s what you can expect upon each announcement.

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Cancer Community Activation Timelines: Are NCI Expectations Achievable?

The NCI sets high standards for protocol activation timelines. While the expectation for protocols to be activated in 8-12 weeks, is it achievable? What can be done to improve study start up time?

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Waiving Informed Consent Under the Proposed Rule

Under the Proposed Rule, minimal risk trials may have the ability to waive informed consent. Explore the benefits and challenges of this rule.

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Q&A Part II: How Protocol Feasibility Assists in Promoting Compliance

In this Q&A, Dr. Wendy Tate answers attendee questions from her webinar “How Protocol Feasibility Assists in Promoting Compliance.”

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Q&A Part I: How Protocol Feasibility Assists in Promoting Compliance

In this Q&A, Dr. Wendy Tate answers attendee questions from her webinar “How Protocol Feasibility Assists in Promoting Compliance.”

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Top 10 Mistakes Made When Conducting Clinical Research

Going through an audit at any clinical research site can be a stressful process. Join us for this educational webinar as Chad Adams, Associate Director at the University of Arizona shares the top 10 mistakes made when conducting clinical research, based on top FDA audit findings.

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PRIM&R AER Conference: Collaborating to Advance Ethical Research

The 2019 PRIM&R AER Conference provided insights into the changing regulatory world, and reaffirmed the importance of technology as processes and regulations continue to evolve.

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3 Tips to Keep in Mind When Preparing for Your Next Audit

At any research site, audits are inevitable. Check out these tips and tricks to help prepare your site for your next audit.

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