See how electronic data capture systems improve information management and analysis and accelerate the timeline for clinical trial approval.

See how 21 CFR Part 820 has the added benefit of embedding GMP that enable safety and optimize operations to prevent costly product failures.

Learn about CDISC, a non-profit organization that develops data standards for clinical data collection, analysis, and exchange.

See how Good Clinical Practice guides studies to ensure that the highest quality data is delivered with the utmost ethical treatment for human subjects.

Learn about electronic consent, considered safe and effective in protecting subjects’ rights in research studies and streamlining study onboarding.

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.