Validation of disinfection procedures for pharma industry

In pharma industry production site that would like or need to change their hygiene regimen, the new established process has to be validated. Based on our phase 3-research project as well as existing standards such as EN 13697 and EN 16615 we can offer such validations with locally in the production site isolated test organisms and surface materials from the site.

Please contact us in case you are interested.