PharPoint Research

Overview

PharPoint Research is a contract research organization (CRO) built on collaborative partnerships with sponsors and study partners. Founded in 2007, the company helps sponsors plan, conduct, and analyze Phase I–IV clinical trials while maintaining transparent communication and efficient study processes.

Core Capabilities

Data Management & Biometrics

• In-house database builders with experience across multiple EDC systems
• Database lock within 5 days of last patient, last visit (LPLV) and final source data verification (SDV)
• Topline results delivery in 2 business days after database lock
• Draft Tables, Listings, and Figures (TLFs) within 5 business days of database lock
• Clinical Study Report (CSR) delivery in 40 business days (assuming two rounds of sponsor review)
• 100% of biostatisticians hold advanced degrees

Clinical Operations & Site Management

• Site identification, activation, and partnership support
• Clinical research associates (CRAs), clinical operations leads (COLs), and project managers (PMs)
• Study physician support integrated into sponsor teams

Regulatory & Medical Support

• Regulatory, clinical, medical, and biometrics consultants
• Medical writing services for study-related documentation
• Data monitoring committee (DMC) setup, member support, and logistics management
• Clinical trial transparency and data cleanliness oversight

Differentiation

PharPoint emphasizes cross-functional alignment to eliminate silos, proactive communication, and consistent delivery of promised timelines. The organization prioritizes early planning, efficient processes, and quality by design.