Directory of Medical Device Standards and Reference Documents PDF Download

Author: Canada. Health Protection Branch
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages :

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Author: Canadian Government Publishing
Publisher:
ISBN: 9780660573168
Category :
Languages : en
Pages : 143

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Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 156

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With 1991: contains domestic, foreign, and international standards for medical devices. Intended for those involved in standards development or interested in specifying safety and performance.

Author: Canadian Hospital Association
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages :

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Author: Canada. Bureau of Radiation and Medical Devices. Standards and Testing Section
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 139

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Author: Canada. Bureau de la radioprotection et des instruments médicaux. Section des normes et des essais
Publisher: Canadian Hospital Association Press = Presses de l'Association des hôpitaux du Canada
ISBN:
Category :
Languages : en
Pages : 139

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Author: Michael Cheng
Publisher: World Health Organization
ISBN: 9241546182
Category : Medical
Languages : en
Pages : 54

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The term 'medical devices' covers a wide range of equipment essential for patient care at every level of the health service, whether at the bedside, at a health clinic or in a large specialised hospital. Yet many countries lack access to high-quality devices, particularly in developing countries where health technology assessments are rare and there is a lack of regulatory controls to prevent the use of substandard devices. This publication provides a guidance framework for countries wishing to create or modify their own regulatory systems for medical devices, based on best practice experience in other countries. Issues highlighted include: the need for harmonised regulations; and the adoption, where appropriate, of device approvals of advanced regulatory systems to avoid an unnecessary drain on scarce resources. These approaches allow emphasis to be placed on locally-assessed needs, including vendor and device registration, training and surveillance and information exchange systems.

Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309038294
Category : Medical
Languages : en
Pages : 709

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For the first time, a single reference identifies medical technology assessment programs. A valuable guide to the field, this directory contains more than 60 profiles of programs that conduct and report on medical technology assessments. Each profile includes a listing of report citations for that program, and all the reports are indexed under major subject headings. Also included is a cross-listing of technology assessment report citations arranged by type of technology headings, brief descriptions of approximately 70 information sources of potential interest to technology assessors, and addresses and descriptions of 70 organizations with memberships, activities, publications, and other functions relevant to the medical technology assessment community.

Author: Amiram Daniel
Publisher: Quality Press
ISBN: 0873897404
Category : Medical
Languages : en
Pages : 355

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How have recent changes in domestic and international regulations affected quality management in the development and marketing of medical devices in the US and abroad? Consultants Daniel and Kimmelman take a close look at the Quality System Regulation (QsReg), the ISO 13485: 2003 standard and the ISO/TR 14969: 2004 guidance document as well as a number of US Food and Drug Administration (FDA) and Global Harmonization Task Force (GHTF) guidance documents. The authors provide extensive commentary and notes an update their material to include such topics as the incorporation of principles of risk management into the medical device organizations' quality management systems (QMSs) and considerations of combination products. Daniel and Kimmelman include full coverage of the QSReg requirements, descriptions of comparable requirements in the ISO documents, excerpts of the FDA's responses to the QSReg preamble and excerpts from FDA guidance documents related to QMSs.

Author: United States. Bureau of Medical Devices
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 48

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