The High Level Structure, well known from the revised ISO 9001:2015, was not adopted in ISO 13485:2016. Medical device manufacturers who wish to use both ISO 13485 and ISO 9001:2015 as a basis for certification must be aware of the differences in structure . On the other hand, this also has the positive aspect that the new ISO 13485 remains familiar in its structure.

作者

Claire Dyson

Loading...

相關文章與活動

你可能對此也感興趣
Blog
Loading...

MDR 協調標準法規更新:委員會實施決定 (EU) 2026/760

Blog
Loading...

2026 EU MDR 最新簡化提案:醫療器械製造商的 5 大核心影響與應對策略

Blog
Loading...

《人工智慧法案》與人工智慧驅動的醫療器械——當前監管現狀