Two people using EDC on computer in a medical clinic

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…

Medical professional using an eCRF on a computer

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…

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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…

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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…

People pointing at numbers on clinical study invoice document

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…

Person drawing a plan for eCRF design on paper

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:…

Two people shaking hands to celebrate Canela Capital acquisition

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…

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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…

Two golden retrievers waiting for lymphoma treatment from VetDC

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,…

Two cows in a cross-species comparative trial

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…

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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…

Auditor in suit giving a thumbs up to clinical study design

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…

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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…

Regulator signing piece of paper to approve clinical trial grant

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…