Blog

IRB Review of Adaptive Design Studies

Learn why the popularity of adaptive design in clinical research is continuing to grow!

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The Six Characteristics of an NCI-Designated Cancer Center

A key component of the CCSG is to demonstrate six major characteristics of an NCI-designated cancer center. Learn more about each characteristic.

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6 Ways Sponsors Can Improve Feasibility Questionnaires

Learn how sponsors can alleviate frustrations when it comes to clinical trial feasibility questionnaires to get the best information from sites.

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“Single IRB” vs “Central IRB” – What’s the Difference?

Is there a difference between the terms sIRB and cIRB?

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The Beginner’s Guide to an Electronic Data Capture (EDC) System

Electronic Data Capture system is software that stores patient data collected in clinical trials. Learn the basics and functionality of an EDC system.

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Deciphering the CRC Career Path: Key Skills and Responsibilities

Interested in becoming a clinical research coordinator? Understand the key skills and experiences sites look for.

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Beginner’s Guide to Clinical Trial Performance Metrics

Learn what clinical trial performance metrics are, why they are important and which key metrics for clinical trials you should be measuring.

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How Paper and Electronic Source Data Meet ALCOA Elements

ALCOA ensures source data is safe and effective, but how does it differ for data collected on paper vs. electronically?

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Best Practices in Pre-Screening Includes Use of Technology

Explore the benefits of pre-screening potential participants before they move on to the informed consent process.

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