Most conversations about AI in maintenance get stuck on definitions. What’s the difference between predictive and generative AI? Which one matters more? These are reasonable [...]
All medicinal manufacturers that distribute within the European Union (EU) must comply with the Good Manufacturing Practice (GMP). Coordinated by the European Medicines Agency (EMA) in partnership with the European Commission, GMP inspections assess whether medicines [...]
Maintaining measurement traceability is a challenge for any organization that must comply with industry-specific regulations for maintenance and testing. However, for those that operate in [...]
Many industries, such as the life sciences, must meet strict regulatory requirements for facility management, equipment validation, and product safety. But that's only part of [...]
Imagine this scenario: A packaging line at a pharmaceutical manufacturer passed performance qualification (PQ) two years ago, and it hasn’t failed a single run since. [...]
The average consumer uses between six and twelve cosmetic products per day, but these products aren’t as heavily regulated by the Food and Drug [...]
For organizations in the life sciences, equipment maintenance plays a critical role in ensuring that products are pure, effective, and safe. When assets aren’t correctly [...]
The pharmaceutical industry is rapidly transforming with the adoption of digital technologies and new, IoT-driven approaches like continuous manufacturing. As organizations pivot to new solutions [...]
Developing a new pharmaceutical drug takes years of research and testing, so when it’s time to move a product to clinical trial, investors are understandably [...]
All improperly calibrated equipment compromises quality, safety, and compliance. But mobile- and field-based assets pose unique challenges. So, what regulations govern calibration compliance in the [...]