A guide for the validation of automated systems in pharmaceutical manufacture.
DQ IQ OQ PQ
Validation protocols are a method of establishing documented evidence that shows a high degree of as...Read more
What is Rotational Cleaning?
EU GMP Annex 1 states that more than one type of disinfecting agent with different modes of action s...Read more
A true cleanroom panel, this system is perfect for projects which need to adhere to GMP guidelines.Read more