Guides
EU MDR: European Union Medical Device…
See how the EU MDR harmonizes requirements across the European Union and provides long-term…Read More
Electronic Data Capture Fundamentals
See how electronic data capture systems improve information management and analysis and…Read More
21 CFR Part 820
See how 21 CFR Part 820 has the added benefit of embedding GMP that enable safety and optimize…Read More
CDISC and CDISC Standards
Learn about CDISC, a non-profit organization that develops data standards for clinical data…Read More
Data Storage
Learn the essentials of data storage and how data storage technology is available to meet nearly…Read More
Good Clinical Practice
See how Good Clinical Practice guides studies to ensure that the highest quality data is…Read More
Electronic Consent: Definition and How It Works
Learn about electronic consent, considered safe and effective in protecting subjects’ rights in…Read More
GxP
See how understanding, implementing, and maintaining GxP standards is an effective way to provide…Read More
Good Laboratory Practice (GLP)
See how GLP principles and fundamental requirements provide the foundation for laboratories to…Read More
18 Data Manipulation Tips
Data manipulation changes the presentation and organization of data. Get data manipulation tips…Read More
Data Reporting
See how to develop and follow proven processes, use accurate raw data, and leverage software…Read More
Credential Stuffing
Learn about credential stuffing, a type of multi-layer cyberattack that “stuffs” stolen usernames…Read More
What Is eCOA? Improving Clinical Trial Data…
Learn about eCOA and how it improves clinical data quality, with benefits that include generating…Read More
