Efficient Clinical Trials

Latest Efficient Clinical Trials Resources

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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Tips for Successful Clinical Trial Budget Negotiations

Effective budget negotiation is consistently a hot topic for clinical research sites. Here are a few tips to make sure your site gets the most from your negotiations.

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How Protocol Feasibility Assists in Promoting Compliance

Wendy Tate, Director of Analytics at Forte, discusses adding a protocol feasibility committee to improve trial compliance and ethics through proper resource allocation and ensuring that the objectives can be met through proper accrual.

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The Beginner’s Guide to Implementing an Enterprise eRegulatory Management System

Many sites understand the benefits of moving from paper regulatory binders to an electronic system. But it’s also important to ensure your organization is implementing a system that will fit your regulatory workflows and set you up for long-term success.

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Performing Protocol Feasibility Assessments to Enhance Clinical Trials

Protocol Feasibilities are designed to help clinical research staff determine the possibility of conducting a study. Here’s how to seamlessly work an assessment in before accepting your next clinical trial.

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Unpacking the Benefits and Drawbacks to eConsent

With electronic processes dominating systems, electronic consent is starting to make its way onto the scene. Check out the benefits and drawbacks to the alternative consent process.

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Informed Consent: When, Why and How It’s Obtained

Conducting informed consent is more than making sure your participants understand the protocol. Learn more about when, why and how it’s obtained continuously throughout a trial.

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Beginner’s Guide to Risk-Based Monitoring

In clinical research, there are many different data points to track and monitor as the trial moves from phase to phase. Learn more about risk-based monitoring and how it fits in with clinical trials.

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