Blog

Recently, the clinical research community has been making efforts to include more diverse subject populations in clinical studies.

eConsent technology can often better inform participants than just the traditional paper consent, which is great from an IRB perspective.

The completion of the human genome project and advances in genetic engineering have paved the way for clinical trials involving human gene transfer

A major element of any IRB review is the examination of potential benefits and risks to study participants.

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

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

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

Is there a difference between the terms sIRB and cIRB?

An Electronic Data Capture system stores patient data collected in clinical trials. Learn the basics & functionality of EDC systems.

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

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