PES supports clinical trials by focusing on endpoint data quality, guaranteeing that your pipeline assets will have the fairest opportunity to demonstrate efficacy, gain approval, and go to market.
Focused On Your Trial’s Success
PES supports several key domains within trials, including endpoint selection, customized web-based training for all site assessors, real-time data quality review, and centralized scoring and grading of patient assessments.Through our integrated set of services, we guarantee the highest quality endpoint data for our clients. Our primary objective is to mitigate trial risk by providing pristine data across sites and assessors. Recognizing that endpoint data quality is foundational to trial success, we customize tools and web-based training to meet specific protocol endpoints.
“PES provides a dynamic service that views nuanced clinical data through the lens of therapeutic expertise and puts that data into a clinical context. They’ve been an invaluable partner.”
Who Is Watching Your Incoming Data?
Your pipeline assets are precious. Yet many clinical trials fail because of inconsistent and incomplete data. The cost? $4 billion goes down the drain annually due to abandoned clinical trials.
If you plan on using a CRO, PES is the independent partner that will assess and validate the endpoint data quality of all your reported data in real time. This is not the function of your CRO. It shouldn’t be. Your CRO should be focused on the things it does well: accrual, regulatory and protocol compliance, and clinical trial management.