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.
Trial Preparation
We serve as an extension of the sponsor’s clinical team, collaborating on all the early planning decisions that can impact the success of a trial study.
Clinical Rater Training
PES designs and deploys web-based training that turns site-based clinicians into effective clinical raters and assessors.
Data Review & Centralized Scoring
PES’s proprietary methods minimize risk and augment accrual, compliance, and retention.
Ancillary Clinical Supplies
PES provides our clients with design, supply, and tracking of ancillary clinical supply kits to support the successful execution of each clinical protocol we work on.
RTQA
PES provides an expert review of radiation therapy treatment plans to confirm uniformity of treatment.
Genomics & Biomarkers
PES is frequently engaged to provide support for biomarker identification and genomics for clinical trials.
Chief Medical Officer, Phase II trial sponsor
“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.
Clinical trials are often derailed by inconsistent or incomplete data - PES is here to help.
The integrity and quality of your clinical trial data is vital to your therapy's success.
CROs don't critically assess the quality and accuracy of your endpoint data - PES does.
