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Edited By Parkinson,Christopher Etc:
Timing of Toxicological Studies to Support Clinical Trials, The - Erstausgabe1994, ISBN: 9780792388722
Taschenbuch
Chicago: AMA, 1914., 1914. Offprint from the Archives of Internal Med., May, 1914, Vol XIII, pp. 673-681. 8vo. 11 pp. Tables. Original printed white wrappers. Covers browned with small ch… Mehr…
The Timing of Toxicological Studies to Support Clinical Trials by C. / Parkinson, Christopher Parkinson - gebrauchtes Buch
ISBN: 9780792388722
The timing of toxicological studies in relation to the clinical evaluation of new medicines is a key topic for strategic planners in the industry and those involved with harmonisation. Re… Mehr…
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1995, ISBN: 0792388720
1994 Gebundene Ausgabe Pharmakologie, clinicaltrial; efficiency; Pharmacology; research; Toxicity, mit Schutzumschlag 11, [PU:Springer Netherlands; Springer Netherland]
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Detailangaben zum Buch - The Timing of Toxicological Studies to Support Clinical Trials (CMR Workshop)
EAN (ISBN-13): 9780792388722
ISBN (ISBN-10): 0792388720
Gebundene Ausgabe
Taschenbuch
Erscheinungsjahr: 1995
Herausgeber: Parkinson, C. McAuslane, N. Lumley, C. Walker, S.R. Springer
172 Seiten
Gewicht: 0,426 kg
Sprache: eng/Englisch
Buch in der Datenbank seit 2007-11-02T15:45:07+01:00 (Zurich)
Detailseite zuletzt geändert am 2023-11-03T00:15:01+01:00 (Zurich)
ISBN/EAN: 9780792388722
ISBN - alternative Schreibweisen:
0-7923-8872-0, 978-0-7923-8872-2
Alternative Schreibweisen und verwandte Suchbegriffe:
Autor des Buches: lumley, parkinson, tim walker
Titel des Buches: the timing toxicological studies support clinical trials, proceedings
Daten vom Verlag:
Autor/in: C. Parkinson; N. McAuslane; C. Lumley; S.R. Walker
Titel: The Timing of Toxicological Studies to Support Clinical Trials
Verlag: Springer; Springer Netherland
150 Seiten
Erscheinungsjahr: 1995-01-31
Dordrecht; NL
Sprache: Englisch
106,99 € (DE)
109,99 € (AT)
118,00 CHF (CH)
Available
XVI, 150 p.
BB; Hardcover, Softcover / Medizin/Pharmazie; Pharmakologie; Verstehen; clinical trial; efficiency; pharmacology; research; toxicity; Pharmacology; Public Health; Public Health und Präventivmedizin; BC
Section I: Introduction and Presentations.- 1 The application of toxicological investigations in the safe development of medicines.- 2 Review of international recommendations on animal toxicity studies and their relation to clinical exposure.- 3 International survey on the timing of toxicity studies in relation to clinical trials.- 4 Considerations for implementing a toxicity testing strategy.- Section II: Personal Views.- 5 Phase I clinical trials: what is the minimum preclinical package necessary for initiating single-dose studies in man? — a toxicologist’s opinion.- 6 Phase I clinical trials: what is the minimum preclinical package necessary for initiating single-dose studies in man? — a clinical pharmacologist’s opinion.- 7 The duration of toxicity studies required to support repeated dosing in clinical investigation —a toxicologist’s opinion.- 8 The duration of toxicity studies required to support repeated dosing in clinical investigation — a clinician’s opinion.- 9 Reproductive and developmental toxicity studies required to support the inclusion of women and children in clinical trials — a toxicologist’s opinion.- Section III: Proposals and the Way Forward.- 10 The minimum non-clinical package for initiating Phase I clinical trials.- 11 The duration of toxicity studies to support repeated dosing in clinical investigation.- 12 The timing of reproductive toxicity studies in relation to clinical trials.- The way forward.- 14 Input to ICH.- Meeting participants.Weitere, andere Bücher, die diesem Buch sehr ähnlich sein könnten:
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