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DescriptionDetails & specsAttachments
This procedure has been created in accordance with ISO 13485:2016, Regulation 2017/745, MDCG 2020-13 (July 2020) and MEDDEV 2.7/1 revision 4.
It can be used by medical device manufacturers in their Quality Management System.
It contains predefined sections and provides recommended guidance for filling in content.
15 pages
It can be used by medical device manufacturers in their Quality Management System.
It contains predefined sections and provides recommended guidance for filling in content.
15 pages
Language
English