Resources & Insights

Get to know PharPoint’s Accounts Receivable Manager, Meg, in this month’s Meet the PharPoint Team feature.

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).

Get to know PharPoint’s Sr. QA Auditor Mital J., in the latest Meet the PharPoint Team series feature.

Discover what an effective DMC charter should look like and what contents are required with PharPoint DMC coordinator Victoria.

Why engage a biostatistician early in the study design process, and how do you identify the right consultant for your study?

Principal Data Manager Shantyana R. gives an inside look at her job responsibilities and shares why she believes PharPoint is not your average CRO.

How can an experienced biostatistician provide critical support before and during the regulatory submission process?

Exploring industry perspectives and insight regarding data monitoring committee member training with PharPoint DMC coordinator Victoria Elder.

Discover key interactions between clinical data management and biostatistics teams for a more efficient clinical trial.

In early 2024, FDA released an updated draft guidance for data monitoring committees (DMCs).