Resources & Insights
Statistical Support for Regulatory Submissions and Confidently Navigating Regulatory Discussions
How can an experienced biostatistician provide critical support before and during the regulatory submission process?
The Rising Need for Data Monitoring Committee Member Training
Exploring industry perspectives and insight regarding data monitoring committee member training with PharPoint DMC coordinator Victoria Elder.
Key Interactions Between Biometrics Teams for a More Efficient Clinical Trial
Discover key interactions between clinical data management and biostatistics teams for a more efficient clinical trial.
A Review of the 2024 Draft Guidance for DMCs
In early 2024, FDA released an updated draft guidance for data monitoring committees (DMCs).
PharPoint Awarded Position on The Triangle Business Journal’s “Best Place to Work” List for 2024
For the second year in a row, PharPoint has been recognized as one of the best places to work in the Raleigh/Durham/Research Triangle Park area.
Meet the PharPoint Team: Alyssa L., Lead Data Manager, Data Management
PharPoint Lead Data Manager Alyssa L. shares more about her role, her career growth, and what she enjoys about working at PharPoint.
Meet the PharPoint Team: Chris W., Proposals Manager
Learn about the Proposals process in the exciting world of CROs from our Proposal’s manager, Chris W.
Exploring the Characteristics of a High-Performing Medical Writing Vendor
What characteristics should you look for in your medical writing partner? We spoke with PharPoint’s Associate Director of Medical Writing, Samia, to learn more.
Meet the PharPoint Team: Jaye F., Operations Assistant
Get to know Operations Assistant, Jaye F. as he walks us though his exciting career story and why he loves working at PharPoint.
6 Questions to Ask a Phase 1 Unit to Ensure Study Success
Asking the right questions is key to determining how successful sites will be in ensuring the overall success of your Phase 1 study.