Data Management

Achieving Expedited Database Lock with Director of DM, Wendy Moffett

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

August 11, 2025
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Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs

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

August 7, 2024
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Key Interactions Between Biometrics Teams for a More Efficient Clinical Trial

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

June 18, 2024
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The Journey of Clinical Trial Data Points: From Patient to TLFs

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

March 9, 2021
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What makes database design “smart”?

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

January 6, 2021
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How to Perform non-eCRF Data Reconciliation

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.

January 9, 2020
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Choosing an EDC Provider: Ask a CRO 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?

January 9, 2020
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PharPoint Incorporates EDC Software Medrio into Data Management Offerings

Explore how PharPoint Research integrates Medrio’s EDC software into its data management offerings to enhance clinical trial efficiency. Discover the benefits of streamlined data collection, improved accuracy, and accelerated study timelines with Medrio’s innovative solutions.

October 9, 2011
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PharPoint joins Medidata Solutions’ CRO partner program

Medidata Solutions announced that PharPoint has joined Medidata’s ASPire to Win® channel partner program.

October 9, 2010
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