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Drugs between research and regulations : proceedings of the 5th International Meeting of Pharmaceutical Physicians, Munich, October 14-17, 1984

Author: C Steichele; U Abshagen; J Koch-Weser; D Lorke; F H Gross
Publisher: Darmstadt : Steinkopff Verlag ; New York : Springer-Verlag, ©1985.
Edition/Format:   Print book : Conference publication : EnglishView all editions and formats
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Genre/Form: Conference papers and proceedings
Congresses
Congrès
Additional Physical Format: Online version:
International Meeting of Pharmaceutical Physicians (5th : 1984 : Munich, Germany).
Drugs between research and regulations.
Darmstadt : Steinkopff Verlag ; New York : Springer-Verlag, ©1985
(OCoLC)564206854
Material Type: Conference publication
Document Type: Book
All Authors / Contributors: C Steichele; U Abshagen; J Koch-Weser; D Lorke; F H Gross
ISBN: 9780387912653 0387912657 3798506574 9783798506572
OCLC Number: 15519341
Notes: "In memoriam Franz Gross"--Preliminary page.
Description: xii, 205 pages : illustrations
Contents: Chronic Concern on Chronic Toxicity Studies.- Chronic toxicity tests, current problems and possible solutions.- What can be gained from a retrospective analysis of chronic toxicity studies?.- The role of carcinogenicity studies in risk assessment.- Alternatives to chronic toxicity studies.- Clinical Trials and Medical Practice.- What good are clinical trials?.- Clinical guidelines - a help or a hindrance?.- Clinical trials in the natural environment.- Clinical trials and the general practitioner.- Clinical trials and chronic diseases.- Alternatives to clinical trials in post-marketing research on drug effects.- The Future of Long-Term Intervention and Prevention Studies.- The future of long-term intervention and prevention studies - methodological aspects.- Lessons for the future from long-term studies with beta blockers and hypolipidaemic agents.- Rauwolfia derivatives and breast cancer: how do we know when we have the answers?.- The organisation of long-term intervention and prevention studies.- New Biostatical Concepts for Clinical Trials.- The explanatory and pragmatic approaches in clinical trials.- Alternatives to classical randomized trials.- Data quality assurance with particular regard to protocol violations.- Clinical Trials in Children.- The need of clinical drug trials in children.- Ethical restrictions in clinical trials in children.- European Drug Registration.- The role of the EEC in the harmonisation of drug registration.- Clinical trials - European recommendations.- Special Lecture.- The Pharmaceutical Industry - research and responsibility.
Responsibility: C. Steichele, U. Abshagen, J. Koch-Weser (eds.) ; with the collaboration of D. Lorke [and others].

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