researchers are evaluating a specimen in a lab

Improving Trial Efficiency Through Protocol Feasibility: Everything You Need to Know

Clinical trials are expensive, and clinicians can’t afford to waste crucial resources when conducting efficient studies. Around 20-50% of studies don’t accrue subjects at the site level, leading to considerable waste in clinical research. Staff productivity levels and monetary resources are significantly affected. The implementation of technology, such as EDC systems, has automated significant processes, leading…

an illustration of a doctor writing on a notepad.

Creating Seamless Data Collection SOPs in Clinical Trials

Accurate and seamless data collection and evaluation are critical to the success of any clinical trial. Clinicians and data managers must implement state-of-the-art systems such as electronic data capture software for seamless data collection. In addition, there should be robust data collection SOPs within the entire trial to ensure consistency and reliability. Here’s a step-by-step guide to…