Data Management

This short video takes a behind-the-scenes look at PharPoint’s 6-8 week standard database build process.

How long does it take to go from final protocol to database go-live?

Explore three common findings from a data management consultant who has experience performing DM CRO oversight.

Director of Data Management Wendy Moffett discusses how PharPoint achieves rapid database lock in this short video.

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).

Discover key interactions between clinical data management and biostatistics teams for a more efficient clinical trial.

Learn more about the journey clinical trial data takes before ending up on the package insert of a drug you’re taking.

What makes database design “smart,” and when should a sponsor start thinking about data collection and analysis? PharPoint programmer Michelle M. explains.

How do you perform non-eCRF data (ECG, Labs, PK) reconciliation in EDC platforms like Medrio? A PharPoint clinical trial expert answers as part of our #askaclinicaltrialexpert blog series.

For our upcoming study, we know we want to use EDC—but there are so many options. How should we choose an EDC provider?