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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....
Mastering the art of validating automated systems: a comprehensive guide to Delta V™
Discover the essentials of validating automated systems in Pharma 4.0. Explore general principles and unique challenges related to Delta V....
ALCOA ++: data integrity and ALCOA
Learn what you need to know about the new ALCOA ++
VALIDATE 2024: digitalization and change in validation
Read this article to explore the key highlights and insights from the VALIDATE 2024 conference, focusing on change management, validation....
Life sciences software: risks and reward of new technology
Onboarding new software into life sciences manufacturing isn’t an easy exercise, but it's worth it. We explain life sciences software....
Your FDA inspection checklist
When you’re being audited or inspected by the FDA, you must be ready for anything. Use our checklist to be....
What’s the difference between an audit and an inspection?
Know the difference between audits, inspections, and assessments.
3 technologies enhancing validation in the life sciences industry
Read this article to explore how technologies like digital validation, AI, and ML are revolutionizing validation in life sciences, enhancing....