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PharPoint's Experience

Leveraging our knowledge for your success

PharPoint Research is experienced in all phases of clinical development from strategic consulting and Phase 1 first-in-man studies to Phase 4 post-marketing studies and patient registries.

Working across all therapeutic areas in multiple countries, PharPoint Research has taken active roles in the development of industry guidelines and the preparation of numerous NDAs. We put our collective experience to work for you by listening to your study needs and holistically selecting experienced team members for every study. Let's make your next clinical trial a success. Contact a PharPoint expert today ≫
Why PharPoint?
Our experience
Our faster timeline
Choosing a CRO
PharPoint Business Repeat Rate

92% business repeat rate

PharPoint EDC tools

Experience with 17+ EDC tools

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PharPoint Business Repeat Rate

All biostatisticians have a masters or PhD

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PharPoint Global Capabilities

Global clinical trial capabilities

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Experience by Phase

PharPoint Research's Experience By Phase

Dedicated Management

  • Each member of PharPoint’s management team possesses 20+ years of industry experience

  • Experts in pharmaceutical, biologic, and device development and clinical trial management

  • PharPoint's management team has worked together for over 12 years

  • Founders have been with the company since the start of operations

  • PharPoint is experienced with over 13 EDC tools

Quick Facts

  • Involved in the preparation of 12 NDA’s during the 2014 fiscal year

  • 1/3 of PharPoint Research’s staff have 16+ years of experience

  • All statisticians have advanced degrees

  • 92% repeat business rate

Team's Operational Experience (in years)

PharPoint Research's Years of Operational Experience

Let our experience and expertise guide your next clinical trial.

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