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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.

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PDF SAFAS Conformity to American FDA 21 CFR part 11
Phone : +377 99 99 52 52
eMail: safas@safas.com
SAFAS - manufacturer of Spectrophotometers (UV, Visible, Atomic Absorption, Infra-Red, Fluorescence), Spectrofluorometers, Luminometers, Multidetection Microplate Readers, Elisa, Analyzers
SAFAS Monaco - Société Anonyme de Fabrication d’Appareillages Scientifiques
Head Offices : 10, quai Antoine 1er - MC 98000 Monaco / Deliveries and pick-up : 9, avenue de la Quarantaine - MC 98000 Monaco
Phone : +377 99 99 52 52 - Fax : +377 99 99 52 50 - Customer service : +377 99 99 52 52 | eMail: safas@safas.com
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