A guide for the validation of automated systems in pharmaceutical manufacture.


Related articles

What is Rotational Cleaning?

Read the whitepaper on how to successfully implement rotational cleaning and why.

Read more

DQ IQ OQ PQ

Validation protocols are a method of establishing documented evidence that shows a high degree of as...

Read more

Monobloc Cleanrooms

A true cleanroom panel, this system is perfect for projects which need to adhere to GMP guidelines.

Read more