Blog

January 26, 2017

Creating feasibility assessments can be as frustrating for sponsors as answering questionnaires is for sites. Here’s how sponsors can alleviate these frustrations, according to sites.

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

January 11, 2017

In 2016, the NIH policy on IRB review for multisite research brought a new-ish term into the clinical research lexicon:...

Is there a difference between the terms sIRB and cIRB?

February 2, 2016

This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.

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

September 17, 2015

Wendy Tate, Director of Data Analytics at Forte, explains key skills and experiences sites look for in a clinical research coordinator.

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

July 11, 2014

Basics to help you get started measuring and improving your clinical trial performance.

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

April 25, 2014

According to the FDA, data should meet certain fundamental elements of quality (ALCOA), whether they’re recorded on paper or electronically.

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

June 21, 2013

Pre-screening subjects is common practice at most sites. In this article, learn some best practices and how technology can play an important role.

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