Conformity to American FDA 21 CFR part 11
Optional software is available for our customers wishing to conform to FDA 21 CFR part 11, particularly enabling to conform to your requirements regarding audit trail, electronic signature, and files and methods protection.
If you are submitted to the American FDA 21CFR part11 requirements, don’t hesitate to ask us, and to send us the list of requirements established by your Quality Insurance services. They will be processed confidentially and promptly.
Our software development engineers are at your disposal to assist you, so as to efficiently and quickly validate your system and fulfil your most stringent requirements.
- PDF SAFAS Conformity to American FDA 21 CFR part 11
The SAFAS Concept of Sustainable Spectroscopy, exclusively reserved to our CustomersConformity to European PharmacopoeiaConformity to European regulations and Directives, and CE markA Quality Manual and a Quality Management System according to ISO9001-2008Certified and connected Standards, and Validation of instrumentsAn exceptional Optical and Mechanical Quality, which built our reputation more than 6 decades of excellenceSAFAS QUARTZ GUARANTEE: Measurements you can rely on