
Why Sites Prefer Prelude EDC – Part 3 – Ease of Navigation
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We consistently get feedback from our clients that their sites prefer working with Prelude EDC. When sites know they will…

Why Sites Prefer Prelude EDC – Part 2 – eCRFs Can Look Just Like Paper
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We consistently get feedback from our clients that their sites prefer working with Prelude EDC. When sites know they will…

Why Sites Prefer Prelude EDC – Part 1 – Integrated Audit Trail
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We consistently get feedback from our clients that their sites prefer working with Prelude EDC. When sites know they will…

Best Practices for eClinical Mid-Study Updates
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There are plenty of reasons it might be necessary to make a change to an Electronic Data Capture system after…

Best Practices for Managing Site Invoicing in Clinical Studies
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Sponsors and CROs invest a lot of time and money in recruiting sites for clinical trial conduct. Sites whose personnel…

Best Practices for eCRF Design – Part 2
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Let’s continue exploring the art of eCRF design with a discussion of additional best practices! In Part 1 we discussed:…

Prelude Dynamics Announces Acquisition by Canela Capital
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Prelude Dynamics, the leading eClinical technology company for animal and human health researchers, announced today that it has been acquired…

Best Practices for eCRF Design – Part 1
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We all know that eCRF design is more of an art than a science. That being said… there are still…

Prelude Partner VetDC Gains Full FDA Approval for TANOVEA® After CVM Remote Access Pilot Program
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VetDC was granted full approval for TANOVEA® (rabacfosadine for injection) for the treatment of lymphoma in dogs on July 15, 2021. This…

Visit Us Virtually at SQA’s 2021 Annual Meeting
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Learn how you can enhance patient compliance via Electronic Patient Reported Outcomes (ePRO). Our Director of Quality Assurance, Ann-Marie Kiser,…

Key Considerations When Running a Cross-Species Comparative Trial
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Did you know 90% of investigational products don’t make it to approval? Why? Because of poor efficacy. One way to…

Field-by-Field Audit Trail – Adopt Early or Not?
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So, how does it work? And how is it different from the standard form-based audit trail? Typically, the audit trail…

How to Design an Auditor Friendly Clinical Study
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Knock, Knock! The BIMO (or FDA QSR) auditor is at the door. It’s time to race around, retrieve documents from…

Thinking Outside of the Box – Your eClinical Technology Partner
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Looking for an EDC vendor who can be flexible and adapt to your needs rather than forcing you into a…

Best Practices in Clinical Trial Application Grantsmanship
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Applying for a clinical trial grant can sometimes feel like turning in a high school English paper. You could turn…