“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
Flexible, consultative clinical trial support THAT HELPS YOU CONDUCT HIGH QUALITY, COST-EFFECTIVE studies FASTER.
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.
EXPERIENCED TEAMS
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.
FASTER TIMELINES
With strategic early planning and collaboration, efficient study processes, and a seasoned study team, PharPoint helps sponsors meet rapid study timelines.
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.
STUDY CONDUCT
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.
EXPLORE OUR RESOURCES
“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)