---
name: PharPoint Research
slug: pharpoint
site: cro
website_domain: pharpoint.com
summary: PharPoint is a US-based CRO specializing in Phase I–IV clinical trials with rapid biometrics timelines, delivering database locks within 5 days of last patient visit and topline results in 2 business days.
tagline: Collaborative CRO delivering rapid clinical trial timelines and transparent study execution.
founded_year: 2007
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: 
tier2_domain_verified: false
updated_at: 2026-06-18T07:00:37.072Z
services_count: 9
modalities_count: 0
indications_count: 0
locations_count: 0
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# PharPoint Research

Collaborative CRO delivering rapid clinical trial timelines and transparent study execution.

Listed on cro.directory.

## Summary

PharPoint is a US-based CRO specializing in Phase I–IV clinical trials with rapid biometrics timelines, delivering database locks within 5 days of last patient visit and topline results in 2 business days.

## At a glance

- Founded: 2007

## Services

- Phase I Clinical Trials
- Phase II Clinical Trials
- Phase III Clinical Trials
- Phase IV / Post-Marketing
- Clinical Operations
- Data Management & eClinical
- Biostatistics & Statistical Programming
- Medical Writing
- Regulatory Affairs

## Long description

## 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.

_Profile last updated: 2026-06-18T07:00:37.072Z. Profile facts may include AI-assisted enrichment._

Auto-generated by BioBM Editorial AI for machine-readable profile access.