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SA HB 13485:2020

[Current]

AS ISO 13485:2017 — Medical devices — A practical guide

The objective of this document is to provide additional insight and understanding of the requirements in AS ISO 13485:2017, Medical devices - Quality management systems - Requirements for regulatory processes.
Published: 17/07/2020
Pages: 191
Content history
Content history
ISO 13485:2016 HB1
DR SA HB 13485:2020

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