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Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 64
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Book Description
Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 64
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Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 47
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Book Description
Author: Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 47
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Book Description
Author: Center for Devices and Radiological Health (U.S.). Office of Training and Assistance
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 38
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Book Description
Author:
Publisher:
ISBN:
Category : Foreign trade regulation
Languages : en
Pages : 332
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Book Description
Author: IBP USA Staff
Publisher:
ISBN: 9781438754109
Category : Business & Economics
Languages : en
Pages : 300
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Book Description
US Drug and Medical Devices Export-Import Regulations Handbook
Author: U. S. Customs and Border Protection
Publisher:
ISBN: 9781304100061
Category : Education
Languages : en
Pages : 0
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Book Description
Explains process of importing goods into the U.S., including informed compliance, invoices, duty assessments, classification and value, marking requirements, etc.
Author:
Publisher:
ISBN:
Category : Commerce
Languages : en
Pages : 220
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Book Description
Author: USA (PRD) International Business Publications
Publisher: International Business Publications USA
ISBN: 9780739729359
Category : Business & Economics
Languages : en
Pages : 404
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Book Description
US Drug and Medical Devices Export-Import Regulations and contacts
Author: Michael Cheng
Publisher: World Health Organization
ISBN: 9241546182
Category : Medical
Languages : en
Pages : 54
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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.
