Proposed United States Food and Drug Administration Laboratory, Irvine, California
Author :
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Page : pages
File Size : 30,5 MB
Release : 1996
Category : Buildings
ISBN :
Author :
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Page : pages
File Size : 30,5 MB
Release : 1996
Category : Buildings
ISBN :
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Page : 270 pages
File Size : 21,90 MB
Release : 1996
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Publisher :
Page : 900 pages
File Size : 34,25 MB
Release : 1971
Category : Administrative law
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Author : United States. Congress. House. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies
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Page : 1548 pages
File Size : 39,11 MB
Release : 2006
Category : Political Science
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Author : United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, and Related Agencies
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Page : 1446 pages
File Size : 40,90 MB
Release : 2000
Category : Medical
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Page : 636 pages
File Size : 10,46 MB
Release : 1995
Category : Environmental impact statements
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Author : Shein-Chung Chow
Publisher : CRC Press
Page : 4031 pages
File Size : 11,71 MB
Release : 2018-09-03
Category : Medical
ISBN : 135111025X
Since the publication of the first edition in 2000, there has been an explosive growth of literature in biopharmaceutical research and development of new medicines. This encyclopedia (1) provides a comprehensive and unified presentation of designs and analyses used at different stages of the drug development process, (2) gives a well-balanced summary of current regulatory requirements, and (3) describes recently developed statistical methods in the pharmaceutical sciences. Features of the Fourth Edition: 1. 78 new and revised entries have been added for a total of 308 chapters and a fourth volume has been added to encompass the increased number of chapters. 2. Revised and updated entries reflect changes and recent developments in regulatory requirements for the drug review/approval process and statistical designs and methodologies. 3. Additional topics include multiple-stage adaptive trial design in clinical research, translational medicine, design and analysis of biosimilar drug development, big data analytics, and real world evidence for clinical research and development. 4. A table of contents organized by stages of biopharmaceutical development provides easy access to relevant topics. About the Editor: Shein-Chung Chow, Ph.D. is currently an Associate Director, Office of Biostatistics, U.S. Food and Drug Administration (FDA). Dr. Chow is an Adjunct Professor at Duke University School of Medicine, as well as Adjunct Professor at Duke-NUS, Singapore and North Carolina State University. Dr. Chow is the Editor-in-Chief of the Journal of Biopharmaceutical Statistics and the Chapman & Hall/CRC Biostatistics Book Series and the author of 28 books and over 300 methodology papers. He was elected Fellow of the American Statistical Association in 1995.
Author : United States. Congress. House. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies
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Page : 454 pages
File Size : 50,40 MB
Release : 2015
Category : Rural development
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Author : United States. Congress. House. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies
Publisher :
Page : 514 pages
File Size : 26,74 MB
Release : 2017
Category : United States
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Author : United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, and Related Agencies
Publisher :
Page : 1614 pages
File Size : 46,37 MB
Release : 1996
Category : Political Science
ISBN :