Regulation of medical devices : a step-by-step guide

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dc.coverageCairo
dc.creatorWorld Health Organization. Regional Office for the Eastern Mediterranean
dc.date2016-08-24T09:10:36Z
dc.date2016-08-24T09:10:36Z
dc.date2016-08-24
dc.date.accessioned2026-08-03T14:31:09Z
dc.description61 p.
dc.descriptionThe purpose of Regulation of medical devices: a step-by-step guide is to improve access by countries to quality and safe medical devices by offering guidance on strengthening their regulatory controls. It provides decision-makers with a roadmap for implementing regulatory systems in their national settings and a step-by-step approach towards the development of national programmes for the regulation of medical devices. It can be applied by any country seeking to develop its regulatory capacity
dc.formatapplication/pdf
dc.identifier9789292745950
dc.identifier1020-041X
dc.identifier9789292745967 (online)
dc.identifierhttps://iris.who.int/handle/10665/249571
dc.identifier.urihttps://repo.dare.co.zw/handle/123456789/267681
dc.languageEnglish
dc.languageen
dc.publisherWorld Health Organization. Regional Office for the Eastern Mediterranean
dc.relationWHO Regional Publications, Eastern Mediterranean Series;38
dc.subjectEquipment and Supplies
dc.subjectQuality Control
dc.subjectOrganization and Administration
dc.titleRegulation of medical devices : a step-by-step guide
dc.typePublications

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