Certification of management systems

NF EN ISO/IEC 17021-1

Certification of such systems by a third party is a means of getting their conformity with international standards recognised, and in this way certifying that the organisation in place meets precise requirements.
The manufacturers of medical devices therefore deploy management systems to satisfy the European regulatory requirements applicable to their activity, particularly in terms of risk management.
Accreditation of the certification bodies constitutes an undeniable advantage for companies benefiting from the certification for their international development, for bidding for RFPs, and for consolidating their skills and technical competence.