95%
repeat business rate
850+
studies participated in since 2007
2 per year
average successful regulatory submissions
> 21 years
average leadership team experience
PharPoint’s clinical leadership team averages 20+ years of experience. We provide efficient study start up, quick enrollment, and quality execution, and offer remote study capabilities.
All PharPoint biostatisticians have advanced degrees. Our wide range of services include study design, DMC support, and in-house custom programming.
By performing data cleaning and reviews on a continuing basis during enrollment and study conduct, PharPoint’s clinical data management team can lock a database within 5 days of LPLV SDV.
The cornerstone of PharPoint Research is our strategic consulting expertise, which is based on our consultants’ involvement in multiple successful development programs.
Explore our infographic library and blog posts or contact a representative for PharPoint’s study-specific experience.