Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
The Resource Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
Resource Information
The item Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies represents a specific, individual, material embodiment of a distinct intellectual or artistic creation found in University of Missouri-Kansas City Libraries.This item is available to borrow from all library branches.
Resource Information
The item Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies represents a specific, individual, material embodiment of a distinct intellectual or artistic creation found in University of Missouri-Kansas City Libraries.
This item is available to borrow from all library branches.
- Summary
- "The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop."--Resource home page
- Language
- eng
- Extent
- 1 online resource (xii, 128 pages)
- Contents
-
- Introduction
- Legislative history of the Medical Device Amendments of 1976
- Premarket notification
- The medical device industry innovation ecosystem
- The global framework for regulation of medical devices
- Public comments
- Isbn
- 9786612885709
- Label
- Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report
- Title
- Public health effectiveness of the FDA 510(k) clearance process
- Title remainder
- balancing patient safety and innovation : workshop report
- Statement of responsibility
- Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
- Title variation
- FDA 510(k) clearance process
- Subject
-
- Congress
- Device Approval -- legislation & jurisprudence -- United States
- Device Approval -- legislation & jurisprudence -- United States -- Congresses
- Device Approval -- standards -- United States
- Device Approval -- standards -- United States -- Congresses
- Electronic books
- Equipment Safety -- standards -- United States
- Equipment Safety -- standards -- United States -- Congresses
- HEALTH & FITNESS -- Holism
- HEALTH & FITNESS -- Reference
- MEDICAL
- MEDICAL -- Alternative Medicine
- MEDICAL -- Essays
- MEDICAL -- Family & General Practice
- MEDICAL -- Holistic Medicine
- MEDICAL -- Osteopathy
- Public health
- Public health -- Equipment and supplies | Standards -- United States -- Congresses
- Public health -- United States -- Congresses
- United States
- United States, Food and Drug Administration
- United States, Food and Drug Administration
- Conference papers and proceedings
- Language
- eng
- Summary
- "The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop."--Resource home page
- Cataloging source
- N$T
- Dewey number
- 610
- Illustrations
- illustrations
- Index
- no index present
- Language note
- English
- LC call number
- RA399.A3
- LC item number
- P83 2010eb
- Literary form
- non fiction
- Nature of contents
-
- dictionaries
- bibliography
- NLM call number
- WB 26
- http://library.link/vocab/relatedWorkOrContributorName
-
- Wizemann, Theresa M
- Institute of Medicine (U.S.)
- Institute of Medicine (U.S.)
- http://library.link/vocab/subjectName
-
- United States
- Public health
- Public health
- Device Approval
- Device Approval
- Equipment Safety
- United States
- MEDICAL
- MEDICAL
- MEDICAL
- MEDICAL
- HEALTH & FITNESS
- MEDICAL
- MEDICAL
- HEALTH & FITNESS
- Public health
- United States
- Label
- Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
- Antecedent source
- unknown
- Bibliography note
- Includes bibliographical references
- Carrier category
- online resource
- Carrier category code
-
- cr
- Carrier MARC source
- rdacarrier
- Color
- multicolored
- Content category
- text
- Content type code
-
- txt
- Content type MARC source
- rdacontent
- Contents
- Introduction -- Legislative history of the Medical Device Amendments of 1976 -- Premarket notification -- The medical device industry innovation ecosystem -- The global framework for regulation of medical devices -- Public comments
- Control code
- 690162710
- Dimensions
- unknown
- Extent
- 1 online resource (xii, 128 pages)
- File format
- unknown
- Form of item
- online
- Isbn
- 9786612885709
- Lccn
- 2012405517
- Level of compression
- unknown
- Media category
- computer
- Media MARC source
- rdamedia
- Media type code
-
- c
- Other physical details
- illustrations (some color)
- Quality assurance targets
- not applicable
- Reformatting quality
- unknown
- Sound
- unknown sound
- Specific material designation
- remote
- System control number
- (OCoLC)690162710
- Label
- Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
- Antecedent source
- unknown
- Bibliography note
- Includes bibliographical references
- Carrier category
- online resource
- Carrier category code
-
- cr
- Carrier MARC source
- rdacarrier
- Color
- multicolored
- Content category
- text
- Content type code
-
- txt
- Content type MARC source
- rdacontent
- Contents
- Introduction -- Legislative history of the Medical Device Amendments of 1976 -- Premarket notification -- The medical device industry innovation ecosystem -- The global framework for regulation of medical devices -- Public comments
- Control code
- 690162710
- Dimensions
- unknown
- Extent
- 1 online resource (xii, 128 pages)
- File format
- unknown
- Form of item
- online
- Isbn
- 9786612885709
- Lccn
- 2012405517
- Level of compression
- unknown
- Media category
- computer
- Media MARC source
- rdamedia
- Media type code
-
- c
- Other physical details
- illustrations (some color)
- Quality assurance targets
- not applicable
- Reformatting quality
- unknown
- Sound
- unknown sound
- Specific material designation
- remote
- System control number
- (OCoLC)690162710
Subject
- Congress
- Device Approval -- legislation & jurisprudence -- United States
- Device Approval -- legislation & jurisprudence -- United States -- Congresses
- Device Approval -- standards -- United States
- Device Approval -- standards -- United States -- Congresses
- Electronic books
- Equipment Safety -- standards -- United States
- Equipment Safety -- standards -- United States -- Congresses
- HEALTH & FITNESS -- Holism
- HEALTH & FITNESS -- Reference
- MEDICAL
- MEDICAL -- Alternative Medicine
- MEDICAL -- Essays
- MEDICAL -- Family & General Practice
- MEDICAL -- Holistic Medicine
- MEDICAL -- Osteopathy
- Public health
- Public health -- Equipment and supplies | Standards -- United States -- Congresses
- Public health -- United States -- Congresses
- United States
- United States, Food and Drug Administration
- United States, Food and Drug Administration
- Conference papers and proceedings
Genre
Member of
- Online access: National Academy of Sciences National Academies Press
- Online access: NCBI NCBI Bookshelf
- Ebook Central Academic Complete
Library Locations
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Data Citation of the Item Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies
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<div class="citation" vocab="http://schema.org/"><i class="fa fa-external-link-square fa-fw"></i> Data from <span resource="http://link.library.umkc.edu/portal/Public-health-effectiveness-of-the-FDA-510k/RzJwR689h-c/" typeof="Book http://bibfra.me/vocab/lite/Item"><span property="name http://bibfra.me/vocab/lite/label"><a href="http://link.library.umkc.edu/portal/Public-health-effectiveness-of-the-FDA-510k/RzJwR689h-c/">Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report, Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies</a></span> - <span property="potentialAction" typeOf="OrganizeAction"><span property="agent" typeof="LibrarySystem http://library.link/vocab/LibrarySystem" resource="http://link.library.umkc.edu/"><span property="name http://bibfra.me/vocab/lite/label"><a property="url" href="http://link.library.umkc.edu/">University of Missouri-Kansas City Libraries</a></span></span></span></span></div>
