Because conventional cleaning methods can risk product loss, biopharmaceutical manufacturers are often reluctant to use PDE/ADE limits to validate cleaning processes. Cleaning validation for biologics ...

Current practices for cleaning and sterilizing biomanufacturing equipment does not differ much between a multi-product versus single-product setting. When it comes to cleaning validation in the ...

Developing a cleaning validation for a reusable medical device presents several challenges. How are you addressing them? "There have been many issues over the last 7 years, so there's increased ...

Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

The various cleaning validation processes adopted by the drug manufacturers in pharma and biopharmaceutical companies is a significant aspect in determining how safe the drugs and medical products ...