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Drug and device product liability litigation strategy / (Record no. 115960)

MARC details
000 -LEADER
fixed length control field 03275cam a2200397 i 4500
001 - CONTROL NUMBER
control field 19826536
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200220074251.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170724s2018 enk b 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2017950105
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780198803539
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
Language of cataloging eng
Description conventions rda
Transcribing agency DLC
042 ## - AUTHENTICATION CODE
Authentication code pcc
043 ## - GEOGRAPHIC AREA CODE
Geographic area code n-us---
050 00 - LIBRARY OF CONGRESS CALL NUMBER
Classification number KF8925.P7
Item number H47 2018
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 346.73038 HER
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Herrmann, Mark,
Relator term author.
245 10 - TITLE STATEMENT
Title Drug and device product liability litigation strategy /
Statement of responsibility, etc. Mark Herrmann, David B. Alden, Geoffrey M. Drake.
250 ## - EDITION STATEMENT
Edition statement Second edition.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Oxford, United Kingdom :
Name of producer, publisher, distributor, manufacturer Oxford University Press,
Date of production, publication, distribution, manufacture, or copyright notice 2018.
300 ## - PHYSICAL DESCRIPTION
Extent lxiii, 406 pages ;
Dimensions 26 cm.
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term unmediated
Media type code n
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term volume
Carrier type code nc
Source rdacarrier
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographical references and index.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Machine generated contents note: -- Acknowledgments -- 1. Introduction -- 2. The FDA's Regulation of Prescription Drugs and Devices -- 3. Pre-litigation Counseling -- 4. Legal Issues & Theories -- 5. Consolidated Proceedings -- 6. Aggregated Proceedings - Class Actions -- 7. Aggregated Proceedings - Multidistrict Litigation -- 8. Fact Discovery -- 9. Expert Retention and Discovery -- 10. Expert Testimony, Rule 702, And Daubert -- 11. Preemption -- 12. The Learned Intermediary Doctrine -- 13. Motions In Limine -- 14. Jury Selection -- 15. The Trial Of A Drug Or Device Case -- Table of Authorities -- Index.
520 ## - SUMMARY, ETC.
Summary, etc. "Each year, thousands of lawsuits are filed in federal and state courts seeking recovery from manufacturers of pharmaceuticals and medical devices. These lawsuits include individual actions, actions consolidated into multidistrict litigation, and class actions. The litigation occasionally becomes life-threatening for the defendant corporations, and may breed a public relations nightmare, as occurred with Vioxx, breast implants, and fen-phen. Drug & Device Product Liability Litigation Strategy, by Mark Herrmann and David B. Alden, offers assistance to lawyers who practice in this high-stakes, high-profile, and rapidly-evolving area. The book's primary focus is to provide useful practice pointers and overall strategic guidance for attorneys involved in product liability litigation for prescription drugs and medical devices. It will serve as an indispensable guide to handling such a case from pre-litigation through trial. The legal landscape in this important area is expected to shift as the Supreme Court's decisions in Riegel v. Medtronic, Inc. and Wyeth v. Levine are applied, and as the President and Congress address tort reform and other health care issues. Practitioners will need thoughtful, expert advice to navigate these changes"--
Assigning source Provided by publisher.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Products liability
General subdivision Medical instruments and apparatus
Geographic subdivision United States
General subdivision Trial practice.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Products liability
General subdivision Drugs
Geographic subdivision United States
General subdivision Trial practice.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Alden, David B.,
Relator term author.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Drake, Geoffrey M.,
Relator term author.
906 ## - LOCAL DATA ELEMENT F, LDF (RLIN)
a 7
b cbc
c origcop
d 2
e epcn
f 20
g y-gencatlg
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type BOOKs
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Materials specified (bound volume or other part) Damaged status Not for loan Collection code Home library Current library Shelving location Date acquired Source of acquisition Coded location qualifier Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification HB     Reference National Law School National Law School   20.02.2020 Purchased REFERENCE   346.73038 HER 37956 20.02.2020 20.02.2020 BOOKs