Medical Devices and Diagnostic Products Standards Survey PDF Download
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Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 232
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Book Description
Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 232
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Book Description
Author: United States. Bureau of Medical Devices
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 240
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Book Description
Author: United States. Bureau of Medical Devices and Diagnostic Products
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages :
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Book Description
Author: United States. Bureau of Medical Devices
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 230
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Book Description
Author: United States. Food and Drug Administration. Bureau of Medical Devices and Diagnostic Products. Division of Medical Device Standards and Research
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages :
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Book Description
Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 156
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Book Description
Author:
Publisher:
ISBN:
Category : Medical instruments and apparatus
Languages : en
Pages : 172
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Book Description
Author: United States. Bureau of Medical Devices and Diagnostic Products
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Author: Annetine C. Gelijns
Publisher: National Academies
ISBN:
Category : Clinical medicine
Languages : en
Pages : 78
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Book Description
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
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Book Description
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
