NF EN ISO 13485/A11

Medical devices - Quality management systems - Requirements for regulatory purposes

Le présent document modifie la NF EN ISO 13485:2016, avec l'intégration de rectificatifs de mars 2016, décembre 2016 et 2018, avec une révision de l'Avant-propos européen et des Annexes européennes ZA et ZB.

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- non-essential but useful clauses to know, such as permissions and recommendations.

The identification of these types of clauses is based on the document “ISO / IEC Directives, Part 2 - Principles and rules of structure and drafting of ISO documents ”as well as on a constantly enriched list of verbal forms.

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