
Navigating 21 CFR Part 11
All companies under the FDA scope must know how to navigate 21 CFR Part 11 for data integrity. We explain....
Resources
All companies under the FDA scope must know how to navigate 21 CFR Part 11 for data integrity. We explain....
Digital validation may be the most important tool for CDMOs to effectively compete in a crowded market. Learn the surprising....
60 minutes
Mo Brar
Learn the importance of equipment validation in the pharmaceutical industry, including the step-by-step process, guidelines, and benefits of digital validation.
Ensure you stay compliant by understanding what data integrity is and the best practices to stay on the right side....
Read this article to discover the essential steps and best practices of cleaning validation in the pharmaceutical and medical device....
Read this eBook to see how to supercharge your cleaning validation process with a digital, data-driven approach. Get expert insights,....
Explore key trends in validation programs from the 2024 State of Validation Report, including CSA adoption rates, resource allocation, and....
Data integrity is crucial to the success of any highly regulated industry. As it evolves, your processes will need to....
Unlock the latest insights and trends in validation practices with the State of Validation Report.