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1,000+
studies supported since 2007
Database lock
1 MONTH
faster than the industry average.
All output delivered
5 days
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Foreseeable factors often unnecessarily jeopardize trial success, and many of these factors can be identified and avoided by an experienced team. One way the PharPoint team proactively recognizes and reduces challenges is through strategic site selection. To accomplish this, we use stringent feasibility assessments, leverage big data and learning algorithms, lean into extensive team experience, and evaluate cross-functional input from stakeholders across the board.
Our team prioritizes your data, with on-going data cleaning to get quality results faster. Additionally, we have partnerships in place with two EDC providers that allow us to build databases in-house and make mid-study changes faster. In total, PharPoint’s data management team has worked in 15+ EDC systems.
Other CROs often use proprietary macros for their programs, which leads to problems for sponsors during the submission process.
At PharPoint, our team uses custom programming and transfers ownership to clients at the end of a study without any added costs. This means that sponsors who partner with us have what they need for submission.
The custom programs we create for you are yours to keep — the way it should be.
Free Interactive Resource
27 Things To Consider During the CRO Selection Process
The right CRO for you is one that is a best match for your individual study needs. While there is no one-size fits all approach, this checklist provides a helpful guide to begin.
SERVICES
PharPoint has supported sponsors with studies from Phase 1 to Phase 4. Our award-winning services include:
Study Rescue
PharPoint experts are an invaluable tool for studies in trouble. Members of our leadership team average 25+ years of clinical research experience. They’ve seen first hand nearly everything that can go wrong in a trial, and have innovative solutions and proactive measures to get your study back on track.
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