Clinical Trial Rescue

PharPoint Research > Services > Clinical Trial Rescue

Working with a "big-box" CRO that's falling behind or failing to deliver results?

PharPoint Research is proud to have been a trusted partner in multiple clinical trial rescue studies. The PharPoint team has taken on various roles as a rescue CRO, including both consultative support and full-scale study remediation.

Partner with a team that’s experienced in overcoming clinical research challenges

PharPoint works with sponsors to uncover the root of study issues, providing innovative solutions to get a study back on track.

Our dedication to quality data and our passion for helping clients improve global health has provided us with broad experience across therapeutic areas and phases.

The PharPoint leadership team is an invaluable tool for studies in trouble, with lived experiences and extensive careers across the CRO and biopharmaceutical industries. Our leadership team averages 20+ years of clinical research experience, with many of those years spent at “big box” organizations. There, they’ve seen first hand nearly everything that can go wrong in a trial, and have brought that insight to PharPoint Research in the form of proactive measures and innovative solutions.

“We’re worried that the service providers working on our study are causing it to fall behind. Timelines are being missed due to slow enrollment and data quality is poor. What are our options?

Don't wait until it's too late to ask for help.

Whether you’re in need of a consultation or full-scale study rescue, PharPoint Research can help your study get back on track.