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

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
Contributor
Author
Subject
Genre
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
LC call number
RA399.A3
LC item number
P83 2010eb
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
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
Publication
Antecedent source
unknown
Bibliography note
Includes bibliographical references
http://library.link/vocab/branchCode
  • net
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
ocn690162710
Dimensions
unknown
Extent
1 online resource (xii, 128 pages)
File format
unknown
Form of item
online
Isbn
9780309162067
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
http://library.link/vocab/recordID
.b26481662
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote
System control number
  • (OCoLC)690162710
  • pebcs0309158508

Library Locations

    • Deakin University Library - Geelong Waurn Ponds CampusBorrow it
      75 Pigdons Road, Waurn Ponds, Victoria, 3216, AU
      -38.195656 144.304955
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