Would you like to get a detailed understanding of the process of validation for regulated industries, with particular focus on validation for the manufacture of medical devices and the requirements of ISO EN 13485.?
If so then be sure to book a place on our Product and Process Validation Course, scheduled for 21st – 25th November 2016
This 5 day course aims to explore in some depth validation activities, the regulatory reasons of these activities and how best to meet these requirements.
