Equipment

Discover how to optimize process plant equipment, from selection to operation to troubleshooting
From energy to pharmaceuticals to food, the world depends on processing plants to manufacture the products that enable people to survive and flourish.

While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives details on how to demonstrate compliance, what data to use, and how to produce the appropriate documentation.

Basic Fundamentals of Welding