Animal Studies: Group-Based vs. Individual Subject Workflows
Planning an animal study’s workflow is an artform. Regulatory aspects such as GLP and GCP should be considered as well…
Best Practices – Leveraging the Biostatistician
We continually urge our Sponsor/CRO clients to make better use of their study Biostatistician. These professionals have more to contribute…
Why Sites Prefer Prelude EDC – Part 3 – Ease of Navigation
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
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
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
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
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
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
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
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
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
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
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?
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
Knock, Knock! The BIMO (or FDA QSR) auditor is at the door. It’s time to race around, retrieve documents from…