Key Considerations when Running a Cross-Species Comparative Trial

Did you know 90% of investigational products don’t make it to approval? Why? Because of poor efficacy.  One way to mitigate the risk of failure before investing too much is to perform cross-species comparative studies, an emerging approach in clinical research....

Best Practices in Clinical Trial Application Grantsmanship

Applying for a clinical trial grant can sometimes feel like turning in a high school English paper. You could turn in the same exact paper on a different day of the month and get very different grades based on factors that seem out of your control (like whether the...

CVM’s Remote Access Pilot Program

CVM’s Office of New Animal Drug Evaluation (ONADE) has launched an initiative that will greatly increase the efficiency of the study submission process. They will now allow submissions through read-only access to online databases in lieu of the submission of copies of...

Announcing VISION™ eConsent!

Announcing eConsent! Prelude’s unique eConsent functionality is the latest in a long line of enhancements aimed at eliminating paper from clinical trials. Up until now, most clinicians have obtained owner and subject consent on paper forms that are then uploaded into...

VISION™’s Invoicing Incentivises Sites

Integrated invoicing is a powerful mechanism for incentivising site participation. It also eliminates extraneous trial management activities. What is it and how does it work? This article takes a closer look at integrated invoicing and how it can work for you.  Sites...