Helping innovative clients meet their clinical trial goals

Get your results over a month faster with the industry-best biometrics timelines PharPoint offers. See how we do it →

Our team is transparent, attentive, and accessible. Our approach →

Learn more about how we’ve worked with companies like yours. SUCCESS STORIES →

studies supported since 2007

Database lock
faster than the industry average.

All output delivered
5 days
after database lock.

You’re an innovator focused on improving global health.

We’re here to support you from pre-IND planning through regulatory approval.

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 (UPDATED MAY 2023)

37 Things To Consider During the CRO Selection Process

The right contract research organization (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.


PharPoint is a contract research organization that supports sponsors from pre-IND planning through regulatory approval. Our award-winning services include:

Clinical Operations & Project Management

PharPoint’s clinical leadership team averages 20+ years of industry experience. We can provide clients support for traditional, virtual, hybrid, and remote clinical trials across a range of therapeutic areas.

Biostatistics & Statistical Programming

PharPoint biostatisticians all have advanced degrees and extensive experience in the CRO industry. Since 2007, our team has supported 30+ successful regulatory submissions.

Data Management

PharPoint’s data management team allows us to bring results to our clients faster than the average CRO. In fact, we’re able to lock a database one month faster than the industry average.

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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