GxP
See how understanding, implementing, and maintaining GxP standards is an effective way to provide safe products and instill confidence in an organization.
See how understanding, implementing, and maintaining GxP standards is an effective way to provide safe products and instill confidence in an organization.
See how GLP principles and fundamental requirements provide the foundation for laboratories to run safely, efficiently, and faster.
Data manipulation changes the presentation and organization of data. Get data manipulation tips for Excel and SQL to make raw data organized and useful.
Learn about eCOA and how it improves clinical data quality, with benefits that include generating more meaningful study reports faster, with less work.
Learn what an eCRF is and see how the transition to eCRFs is driven by the time they save and the transparency they provide in the clinical study process.
See how electronic laboratory notebooks can provide a strategic and competitive edge by up-leveling information capture, workflow optimization, and more.
See how the improvements and cost savings in the lifecycle of a clinical trial far outweigh the time, money, and effort required to implement an eTMF.
See how clinical data management processes that weave through an entire clinical study result in high-integrity data for use in research and reporting.
Case report forms are critical to the quality and efficacy of data collection. Learn about case report forms, including design principles and challenges.
This report from MIT Technology Review Insights highlights how AI accelerates drug development.