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QMS and quality standards

 

DIS-PAR operates an ongoing Quality Management System that monitors and manages all internal management operations and oversees all external inspections. All this is audited and approved by the Bureau Veritas Certification quality standard.

Having obtained ISO 9001:2008 and ISO 13485:2012 certifications for its Quality Management System, DIS-PAR constantly monitors its operations for the purposes of continuous improvement.

DIS-PAR is audited and validated by the relevant Notified Bodies with regard to CE marking for medical devices, DIS-PAR being a ‘manufacturer’ as defined by EC Directive 93/42 concerning medical devices.