Utilize PharPoint’s infographic resource library to find concise one-pagers about our flexible service capabilities, unique advantages, and functional expertise.


How does your current CRO match up to PharPoint’s standard biometric timeline?

PharPoint’s award-winning data management and biostatistics teams pride themselves on bringing results to sponsors faster than the average CRO. Complete the form below for access to our visual timeline.

Capabilities + Expertise Overview →
Get to know PharPoint Research, our capabilities, and what makes our team so unique. View our service overview PDF.

Remote Study Capabilities →
Need a CRO that can handle a fully remote or hybrid trial? Access our remote study capabilities infographic for more information.

Infectious Disease Experience →
Looking for an infectious disease CRO? Access our experience overview.

Oncology Experience →
Looking for an oncology CRO? Access our experience overview.

Biometric Experience →
Learn more about our biostatistics, statistical programming, and data management experience and capabilities.

Global Service Solutions →
Interested in learning more about PharPoint’s global capabilities? Download the infographic for an overview.

Faster Database Lock →

How does PharPoint’s standard biometric timeline compare to the industry average? Access our LPLV to Database Lock timeline to get the comparison.

COVID-19 Experience →
Looking for a CRO with a strong background in infectious disease and growing experience with COVID-19 studies? View our experience overview.

Our team’s experience →
Learn more about the PharPoint Research team, unique qualifications and industry-best expertise.

Clinical Operations Overview →
Learn more about our project management, study startup, and clinical monitoring experience and capabilites.

Cardiovascular Experience →
Looking for a cardiovascular CRO? Access our experience overview.

Case study: Tight Timelines →
In a study rescue, a sponsor brought on PharPoint experts to make 1 SDTM and 1 ADaM dataset and corresponding documentation in the timeline requested by the FDA — 5 days.

Can’t find the information you’re looking for?

Our team is happy to help. Contact us and our team can prepare a customized one-pager, slide deck, or set up a meeting so you can better evaluate how PharPoint can assist your upcoming or on-going study.