Coverart for item
The Resource Challenges for the FDA : the Future of Drug Safety : Workshop Summary, Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Institute of Medicine of the National Academies ; Leslie Pray and Sally Robinson, rapporteurs

Challenges for the FDA : the Future of Drug Safety : Workshop Summary, Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Institute of Medicine of the National Academies ; Leslie Pray and Sally Robinson, rapporteurs

Label
Challenges for the FDA : the Future of Drug Safety : Workshop Summary
Title
Challenges for the FDA
Title remainder
the Future of Drug Safety : Workshop Summary
Statement of responsibility
Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Institute of Medicine of the National Academies ; Leslie Pray and Sally Robinson, rapporteurs
Creator
Contributor
Subject
Genre
Language
eng
Member of
Cataloging source
CaPaEBR
Dewey number
615/.19
Illustrations
illustrations
Index
no index present
Language note
English
LC call number
RM301.27
LC item number
.S96 2007eb
Literary form
non fiction
http://bibfra.me/vocab/lite/meetingDate
2007
http://bibfra.me/vocab/lite/meetingName
Symposium on the Future of Drug Safety: Challenges for the FDA
Nature of contents
  • dictionaries
  • bibliography
NLM call number
  • 2007 L-855
  • QV 771
NLM item number
S9889c 2007
http://library.link/vocab/relatedWorkOrContributorName
  • Pray, Leslie A
  • Robinson, Sally
  • Institute of Medicine (U.S.)
http://library.link/vocab/subjectName
  • United States
  • Drugs
  • Drugs
  • United States
  • United States
  • Drug-Related Side Effects and Adverse Reactions
  • United States Food and Drug Administration
  • Drug Approval
  • Drug Approval
  • Drug-Related Side Effects and Adverse Reactions
  • Drug Approval
  • Safety
  • Product Surveillance, Postmarketing
  • Drug-Related Side Effects and Adverse Reactions
  • Product Surveillance, Postmarketing
  • Adverse Drug Reaction Reporting Systems
  • Drug Evaluation, Preclinical
  • Drug Interactions
  • Government Agencies
  • United States
  • United States
  • MEDICAL
  • MEDICAL
  • MEDICAL
  • MEDICAL
  • Drugs
  • Drugs
  • United States
Label
Challenges for the FDA : the Future of Drug Safety : Workshop Summary, Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Institute of Medicine of the National Academies ; Leslie Pray and Sally Robinson, rapporteurs
Instantiates
Publication
Bibliography note
Includes bibliographical references (pages 78-79)
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
Addressing the FDA's Resource Challenges -- Strengthening the Scientific Base of the Agency -- Integrating Pre- and Postmarket Review -- Enhancing Postmarket Safety Monitoring -- Conducting Confirmatory Drug Safety and Efficacy Studies -- Enhancing the Value of Clinical Trial Registration -- Enhancing Postmarket Regulation and Enforcement -- Looking to the Future
Control code
290490622
Dimensions
unknown
Extent
1 online resource (xvii, 109 pages)
Form of item
online
Isbn
9786611093556
Lccn
2008299141
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations
Specific material designation
remote
System control number
(OCoLC)290490622
Label
Challenges for the FDA : the Future of Drug Safety : Workshop Summary, Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Institute of Medicine of the National Academies ; Leslie Pray and Sally Robinson, rapporteurs
Publication
Bibliography note
Includes bibliographical references (pages 78-79)
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
Addressing the FDA's Resource Challenges -- Strengthening the Scientific Base of the Agency -- Integrating Pre- and Postmarket Review -- Enhancing Postmarket Safety Monitoring -- Conducting Confirmatory Drug Safety and Efficacy Studies -- Enhancing the Value of Clinical Trial Registration -- Enhancing Postmarket Regulation and Enforcement -- Looking to the Future
Control code
290490622
Dimensions
unknown
Extent
1 online resource (xvii, 109 pages)
Form of item
online
Isbn
9786611093556
Lccn
2008299141
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations
Specific material designation
remote
System control number
(OCoLC)290490622

Library Locations

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