Resources

Efficient Clinical Trials

Latest Efficient Clinical Trials Resources

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.

Read more

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.

Read more

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.

Read more

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.

Read more

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.

Read more

Creating new efficiencies through multi-site regulatory data exchange

Coordinating centers  often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management System.

Read more

3 Ways to Improve Your Relationship with Your IRB

Mitigating tension with your IRB comes down to communication. This can make all the difference in your experience conducting research. Here are a few tips you can implement today in order to streamline the approval process.

Read more

Leveraging Community to Move the Clinical Research Industry Forward

Actively participating in the clinical research community can help you address your institutions biggest challenges, while working together with your peers to truly move clinical research forward.

Read more

Good Clinical Practice: What It Is, Why It’s Important and How to Achieve It

Good Clinical Practice benefits research in more ways than complying with the Food and Drug Administration. Learn more about why it’s important and how it helps achieve best practices of any clinical trial.

Read more

Driving Technology Adoption and Preparing End-Users for Success

In this webinar, Kathleen O’Malley, Associate Director of Education and Training at Jefferson Clinical Research Institute and Paul Park, Manager of Clinical Research Systems at City of Hope will discuss robust strategies to drive technology adoption with an emphasis on training practices designed to prepare end users for success.

Read more

1 2 3 7