What the CDMO cell and gene therapy landscape tells us about the future of validation
Validation requirements are different for CDMOs in Cell and Gene Therapy development — but there are ways to make it....
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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....
Equipment validation in the pharmaceutical industry
Learn the importance of equipment validation in the pharmaceutical industry, including the step-by-step process, guidelines, and benefits of digital validation.
What is data integrity?
Ensure you stay compliant by understanding what data integrity is and the best practices to stay on the right side....
Cleaning validation
Read this article to discover the essential steps and best practices of cleaning validation in the pharmaceutical and medical device....
The evolving landscape of validation programs in 2024
Explore key trends in validation programs from the 2024 State of Validation Report, including CSA adoption rates, resource allocation, and....
Insights from the 2024 state of validation report: people and organizations
Read this article to discover key findings from the 2024 State of Validation Report, including trends in team sizes, outsourcing,....
Paperless validation
Read our blog to discover the benefits of paperless validation, streamlining operations and promoting sustainability.
Explaining CQV, C&Q, and commissioning and qualification
CQV, C&Q, and commissioning and qualification, are they all the same? We explore this crucial part of manufacturing in this....