Ideas that matter

Filling in the Knowledge Gaps of a Clinical Trial Site Monitoring Team

You’ve spent countless hours of preparation setting up your clinical trial, finding the right team to staff it, and have set the final pieces into motion. But no matter how meticulous you’ve been in the pre-trial process, there is still no certainty that the trial will run smoothly. At worst, you don’t want to be another statistic [...] Read More

ICH E6 (R2) Training Strategies That Combat the Forgetting Curve

Clinical trials with human subjects are regulated by several different national and international organizations to protect the safety and welfare of human subjects in clinical research. In particular, the International Conference on Harmonisation (ICH) provides the research community with Good Clinical Practice guidelines (GCPs), a set of [...] Read More

Managing Your Risks – 3 Ways To Strengthen Your Clinical Trial Site Monitoring Program

Pharma companies, sponsors and contract research organizations are under tremendous pressure to bring new products to market safely, on time, on budget, and in compliance with the stringent Guideline for Good Clinical Practice (GCP) set out by International Council for Harmonization’s (ICH) E6(R2). The process is complex and the r [...] Read More

Boost Your Patient Safety Training Program In 3 Minutes a Day

What if clinicians could improve the lives of their patients by engaging in a simple game on their smartphone in just three minutes a day? It’s pretty powerful to think about. According to the World Health Organization (WHO), there is a 1 in a million chance of a person being harmed while traveling by plane, and a 1 in 300 chance of [...] Read More