Author: Publisher:
ISBN:
Category : France
Languages : en
Pages : 16
Book Description
France
Author: Publisher:
ISBN:
Category : France
Languages : en
Pages : 16
Book Description
Finance and Supply
Author: United States. Surgeon-General's OfficePublisher:
ISBN:
Category : World War, 1914-1918
Languages : en
Pages : 944
Book Description
Monthly Catalog of United States Government Publications
Author: Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 628
Book Description
Cumulative Index to Foreign Market Surveys
Author: United States. Bureau of International CommercePublisher:
ISBN:
Category : Export marketing
Languages : en
Pages : 124
Book Description
International Commerce
Author: Publisher:
ISBN:
Category : Consular reports
Languages : en
Pages : 642
Book Description
Monthly Catalogue, United States Public Documents
Author: Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 836
Book Description
Cumulative Index to Foreign Production and Commercial Reports
Author: United States. Bureau of International CommercePublisher:
ISBN:
Category : Commerce
Languages : en
Pages : 248
Book Description
Cumulative Index to Foreign Market Surveys Available in Foreign Production and Commercial Reports
Author: Publisher:
ISBN:
Category : United States
Languages : en
Pages : 44
Book Description
Checklist of BFC Publications
Author: United States. Bureau of Foreign CommercePublisher:
ISBN:
Category : International trade
Languages : en
Pages : 638
Book Description
Medical Device Regulations
Author: Michael ChengPublisher: World Health Organization
ISBN: 9241546182
Category : Medical
Languages : en
Pages : 54
Book Description
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.
