Have confidence in your CROs ability to support your study seamlessly.

PharPoint provides attentive, experienced clinical and biometrics support for innovative clients of all sizes.


Efficiently and strategically plan, execute, and analyze Phase 1 – Phase 4 clinical trials with support from our experts.

PharPoint was founded in 2007 with a rebellious spirit and a firmly focused mission: to create an alternative to rigid, unimaginative, quality-compromised clinical research organizations. We’re proud to have supported innovative clients for 1,000+ clinical trials over the past 15 years, including 30+ successful regulatory submissions.

Helping innovative clients improve global health

PharPoint provides clients with full-service CRO support. Contact our business development team to learn more about how we can better support your current or upcoming clinical trial.


Hear what our clients and partners have to say

“There is an inherent honesty and authenticity in [PharPoint’s] approach. …I have complete faith and trust in PharPoint as our partner, and that gives me confidence in the success of our clinical program.”

Client, Pharmaceutical Company

“I can highly recommend partnering with PharPoint.  Not only were documents provided to our site in a timely manner, communication with all parties from the CRA to the project managers has been excellent.”

Partner, Study Coordinator

“…High priority pivotal studies locked and delivered faster than any other CRO I have worked with in my experience. Not only was the study delivered within budget and early, it was a quality deliverable.”

Client, Biotechnology Company