Guidelines foe Evaluation of Medical Devices and In Vitro Diagnostic Medical Devices According to the Regulation Of The Minister of Health of The Republic of Indonesia Number 62 of 2017

Publikasi Sttind

dc.contributor.author	Indonesia, Kementerian Kesehatan Republik Indonesia. Direktorat Jenderal Kefarmasian dan Alat Kesehatan
dc.date.accessioned	2023-06-06T06:13:57Z
dc.date.available	2023-06-06T06:13:57Z
dc.date.copyright
dc.date.issued	2022-04-16
dc.identifier.isbn	9786233010252
dc.identifier.isbn
dc.identifier.issn
dc.identifier.other	000689
dc.identifier.uri
dc.identifier.uri	https://repo.stikes-ibnusina.ac.id/xmlui/handle/123456789/184
dc.description.abstract
dc.format	Text
dc.language	Indonesia
dc.publisher	Kementerian Kesehatan RI
dc.subject.ddc	610.28
dc.subject.ddc	610.28
dc.title	Guidelines foe Evaluation of Medical Devices and In Vitro Diagnostic Medical Devices According to the Regulation Of The Minister of Health of The Republic of Indonesia Number 62 of 2017
dc.type	Textbook

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