Clinical Data Management Services

PharPoint’s highly experienced clinical data management team prioritizes your data, working proactively and cross-functionally to expedite timelines after last patient, last visit.

Our clinical data management services include:

  • Study oversight and flexible consulting support
  • Study tools development
  • Comprehensive data management plans
  • EDC system selection
  • Database development, validation, and testing
  • Medical data coding
  • Global data entry, cleaning, and verification
  • Data import and data export specification preparation
  • Data processing for paper and EDC studies
  • Data standardization

Database lock 31 days faster than the industry average

With PharPoint, database lock occurs within 5 days of LPLV SDV. By initiating data reviews at the beginning of and throughout a study’s life cycle, we can address data discrepancies as they occur and send site queries immediately instead of waiting until the end of a study. This allows for faster timelines, fewer site query errors, and identification of trends early on to increase data cleanliness.

Get study results faster: explore our industry-leading biometrics timelines.

Faster database builds & mid-study changes

Work with our in-house, accredited database programmers.

In addition to having experience with 15+ EDC systems, PharPoint has accredited database programmers for EDC systems Medidata RAVE & Medrio, resulting in faster database development timelines.

Databases are typically constructed based on sponsor provided eCRF prototypes or study requirement specifications, but PharPoint can incorporate clinical data acquisition standards harmonization (CDASH) standards if prototypes or specifications are not provided.

Better communication and more efficient clinical trials

Our data management team is in constant communication with the clinical operations and biostatistics teams, disseminating and maintaining study-related knowledge across teams. This mitigates the risk of errors by establishing study objectives and assignments at the beginning of a study, and ensuring better communication throughout.

Supporting Global Clinical Trials

PharPoint’s data management team has worked with sites in 30+ countries across 6 continents.