For both paper and EDC based trials
With an error rate of less than 0.1%, PharPoint’s data management team instills confidence in our sponsors. We offer an array of data services for both paper and EDC based trials. Our skilled team is equipped to handle small, single site studies and large-scale, international studies.
Through reliable and secure data processes using the industry’s leading technology for data capture, we design and build databases with full consideration of study data tabulation model (SDTM) and clinical data acquisition standards harmonization (CDASH) best practices. PharPoint’s highly experienced data management and database programming teams take pride in recommending efficient data management and programming solutions for your study. All PharPoint databases are subject to the highest data quality standards and must pass a database audit.
Time is often a sponsor's most limited resource, so PharPoint works diligently to deliver results faster than our competitors without compromising quality. View our standard timeline.
Tania Sholar, Principal Data Manager IITania Sholar has been in data management since 2000, with a wide breadth of therapeutic areas (including anti-viral, musculoskeletal, dermatology, oncology, neurology, ophthalmology, cardiovascular, urology, nephrology, respiratory, immunizations, circulatory, endocrinology, and devices). Tania has been an instrumental Program Manager/Lead Data Manager in all aspects of a clinical trial, from feasibility through archiving.