We use cookies to help give you the best experience on our site. By continuing, you agree to our use of cookies. Learn more about how they improve your experience.
A guide for the validation of automated systems in pharmaceutical manufacture.
Gerelateerde artikelen
Wat is roterende reiniging?
Hoe rotatie-reiniging succesvol kan worden geïmplementeerd en waarom
Lees verderDQ IQ OQ PQ
Validation protocols are a method of establishing documented evidence that shows a high degree of as...
Lees verderMonobloc paneelsystemen
Een monobloc cleanroom paneelsysteem is het best in staat om de betere ISO 14644-1:2015 classificati...
Lees verder