At Clean Cells, quality assurance, whether scientific or regulatory, is a reality and is applied every day by all our teams. It is the full-time job of a Quality Director, Industrial Biology engineer and two Quality Assistants to ensure that the company’s quality assurance policy is continuously implemented and improved. The team has the strong backing of the Clean Cells Management Committee, which is very committed to the subject.

A quality management system has been set up in the company, with specific rules that meet the requirements of the following:

 

 

1. the standard NF EN ISO 9001: 2008
2. the Pharmacopoeia guidelines
3. the principles of Good Laboratory Practice (GLP)
4. Good Manufacturing Practice (GMP)

                 

This quality management system is set down in writing in our ’Quality Manual’, which is regularly updated. Our Management Committee makes sure that its contents are known, understood, implemented, respected and improved by all Clean Cells’ personnel.