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Quality Management System Requirements 2016
Quality Management System Requirements 2016, Total:9 items.
In the international standard classification, Quality Management System Requirements 2016 involves: Company organization and management, Quality, Medical equipment.
Danish Standards Foundation, Quality Management System Requirements 2016
- DS/EN ISO 13485:2021 Medical devices – Quality management systems – Requirements for regulatory purposes (ISO 13485:2016)
German Institute for Standardization, Quality Management System Requirements 2016
- DIN EN ISO 13485/A1:2019 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German and English version EN ISO 13485:2016/prA1:2019
- DIN EN ISO 13485:2021-12 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016 + AC:2018 + A11:2021
- DIN EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016
- DIN EN ISO 13485:2021 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016 + AC:2018 + A11:2021
- DIN EN ISO 13485 Berichtigung 1:2017 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016, Corrigendum to DIN EN ISO 13485:2016-08; German version EN ISO 13485:2016/AC:2016
TIA - Telecommunications Industry Association, Quality Management System Requirements 2016
CN-STDBOOK, Quality Management System Requirements 2016
- 图书 3-8304 Understanding and Implementation of GB/T 19001-2016 "Quality Management System Requirements"
European Committee for Standardization (CEN), Quality Management System Requirements 2016
- EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)