Helping innovative clients meet their clinical trial goals

From pre-IND to approval, get attentive, experienced support from a consultative contract research organization (CRO).

“There is an inherent honesty and authenticity in their approach, and as a result, I have complete faith and trust in PharPoint as our partner, and that gives me confidence in the success of our clinical program.”

— US General Manager, Biotechnology Client

“…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.”

— VP Clinical Operations, Pharmaceutical Client

Meet the contract research organization that your entire team will love working with.

Flexible, consultative clinical trial support THAT HELPS YOU CONDUCT HIGH QUALITY, COST-EFFECTIVE studies FASTER.

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INCREASED Transparency

Transparency and good business ethics are at the heart of everything we do: from the proposal process to how we communicate on-going study progress.

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The PharPoint team has supported 1,000+ clinical trials and aligns clients with study team members that have the right knowledge and expertise to meet study goals.

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With strategic early planning and collaboration, efficient study processes, and a seasoned study team, PharPoint helps sponsors meet rapid study timelines.


Receive tailored insight that complements your expertise.

Looking for a clinical consultant to help set your study up for success? PharPoint’s consulting services include pre-IND meeting support, strategic site identification, and enrollment predictions.


Start enrolling faster with an expedited study start up.

Our team works diligently alongside other study partners and sites to get your study off the ground quickly. We leverage a tiered activation process to prioritize FPI. PharPoint is also a registered member of the Accelerated Clinical Trial Agreement (ACTA) and can expedite the contract negotiation process with other participating institutions.


Keep your study on track and in compliance.

Enroll patients through partnerships with sites invested in study success, be confident in compliance with a team of experienced monitors and clinical leads, and overcome challenges as they arise with nimble support from clinical trial experts.


Get results one month faster than industry average.

Experience an expedited database lock, get topline results quickly, and feel prepared for next steps – whether that’s the next phase, a regulatory submission, or the next project.


We’re transparent, attentive, & consultative. But don’t just take our word for it.

“My experience working with PharPoint has been a pleasure. They have taken ownership of our clinical trial since day one. I truly feel that we work as one team.”

– Sr. Director, Clinical Operations (Biotech Client)

Interactive Checklist: 37 Considerations for Selecting a CRO