New EDC Feature for POC and Phase 1 studies

Prelude announces a new EDC feature that streamlines data entry for Proof of Concept (POC) or Phase 1 studies. Multiple Subject Data Entry allows users to enter data for multiple subjects at the same time using a single form. Users can configure this form at the site...

Performing a Remote Audit of your EDC Vendor

There has been a great deal of discussion lately on remote trials, remote monitoring, e-consent, etc., in the context of COVID-19. Another great topic worth discussing is remote auditing. Sponsors and CROs typically conduct on-site audits of their EDC vendors on a...

Announcing Source Data Verification in VISION EDC

Source Data Verification  Prelude Dynamics continues to enhance our VISION™ platform with crucial features requested by our clinical trial user community. The ability to perform Source Data Verification (SDV) in the context of EDC has become more and more important...

Best Practices for Remote Clinical Monitoring 

What does it mean to conduct effective remote clinical monitoring? It’s critical to be using an EDC in order to accomplish this, but what else is necessary? Keeping the primary goals of the monitor in mind, we will outline several techniques for streamlining this...

New Reality of Remote Audits

This morning, Prelude attended a meeting on the new reality of remote audits and inspections. In the past, remote auditing of sites was viewed as a nice capability. As many in the industry are now learning, remote capabilities are now a necessity.

Prelude Registry Featured on Animal Planet

We were excited to see that the Great Ape Heart Project (GAHP) was featured in an episode of Animal Planet’s “The Zoo – San Diego”! Cardiovascular disease has long been recognized as an issue for Great Apes, and the GAHP registry is used to record and monitor the...

How to Make the Most of Remote Trials During COVID-19

For years, technology’s detractors have bemoaned the loss of in-person interaction. While we admit this has been an issue on occasion, it’s now an asset to moving important clinical research forward.  Many human and animal health studies are either still done on paper...

How NOT to Design eCRFs

There are so many ways to design electronic CRFs. Perhaps by looking at how NOT to design them, we can come up with some fresh ideas for how to make your next study a smashing success.
Fail to consider how well the forms will function on handheld devices.

Your 5-Minute Guide to Digital Paper

The main purpose of Digital Paper is to give investigators in the field a place to synchronously record their findings as they perform physical exams on animals in places where there is limited internet available (e.g., horses out in the country) without having to write it on physical paper then transcribe it later.

Mid-Study Updates: Where Can a Batch Edit Check Play a Part?

Have you ever worried about how a mid-study update to calculations or constraints might be implemented without affecting any previously entered data? Hopefully, this overview of batch edit checks will give you a good idea what options are available to you when...