(2017). HRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018): HRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018). Zagreb: Hrvatski zavod za norme.
Chicago stil citiranjaHRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018): HRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018). Zagreb: Hrvatski zavod za norme, 2017.
MLA stil citiranjaHRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018): HRN EN ISO 13485:2016/Ispr.2:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (EN ISO 13485:2016/AC:2018). Zagreb: Hrvatski zavod za norme, 2017.