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Edited By Parkinson,Christopher Etc:

Timing of Toxicological Studies to Support Clinical Trials, The - Pasta blanda

2008, ISBN: 9780792388722

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Edited By Parkinson,Christopher Etc:

Timing of Toxicological Studies to Support Clinical Trials, The - Primera edición

1994, ISBN: 9780792388722

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The Timing of Toxicological Studies to Support Clinical Trials by C. / Parkinson, Christopher Parkinson - C. / Parkinson, Christopher Parkinson
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C. / Parkinson, Christopher Parkinson:
The Timing of Toxicological Studies to Support Clinical Trials by C. / Parkinson, Christopher Parkinson - libro usado

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… Más…

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Timing of Toxicological Studies to Support Clinical Trials : Proceedings : C. M. R. Discussion Meeting on the Timing of Toxicological Studies (1994 : Nutfield, - Christopher Parkinson
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Christopher Parkinson:
Timing of Toxicological Studies to Support Clinical Trials : Proceedings : C. M. R. Discussion Meeting on the Timing of Toxicological Studies (1994 : Nutfield, - libro usado

1994, ISBN: 9780792388722

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The Timing of Toxicological Studies to Support Clinical Trials - Parkinson, C. (Herausgeber); Walker, S. R. (Herausgeber); Lumley, C. (Herausgeber); McAuslane, N. (Herausgeber)
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Parkinson, C. (Herausgeber); Walker, S. R. (Herausgeber); Lumley, C. (Herausgeber); McAuslane, N. (Herausgeber):
The Timing of Toxicological Studies to Support Clinical Trials - encuadernado, tapa blanda

1995, ISBN: 0792388720

1994 Gebundene Ausgabe Pharmakologie, clinicaltrial; efficiency; Pharmacology; research; Toxicity, mit Schutzumschlag 11, [PU:Springer Netherlands; Springer Netherland]

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Detalles del libro
The Timing of Toxicological Studies to Support Clinical Trials (CMR Workshop)

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. Resolving the anomalies between different regulatory authorities should eliminate redundant testing on animals and improve the efficiency of the developmental process by encouraging single international strategies. To aid industry in reaching a consensus, the Centre for Medicines Research brought together representatives of the pharmaceutical industry from Europe, Japan and the U.S.A., to give a comprehensive account of current international industry positions on the subject. The contributions review the situation and address the clinical and strategic requirements of the preclinical programme. Personal and consensus proposals on the toxicity studies required to initiate clinical investigations, the timing of reproductive toxicity tests and the duration of repeat-dose studies to support clinical development are provided.

Detalles del libro - The Timing of Toxicological Studies to Support Clinical Trials (CMR Workshop)


EAN (ISBN-13): 9780792388722
ISBN (ISBN-10): 0792388720
Tapa dura
Tapa blanda
Año de publicación: 1995
Editorial: Parkinson, C. McAuslane, N. Lumley, C. Walker, S.R. Springer
172 Páginas
Peso: 0,426 kg
Idioma: eng/Englisch

Libro en la base de datos desde 2007-11-02T08:45:07-06:00 (Mexico City)
Página de detalles modificada por última vez el 2023-11-02T17:15:01-06:00 (Mexico City)
ISBN/EAN: 0792388720

ISBN - escritura alterna:
0-7923-8872-0, 978-0-7923-8872-2
Mode alterno de escritura y términos de búsqueda relacionados:
Autor del libro: lumley, parkinson, tim walker
Título del libro: the timing toxicological studies support clinical trials, proceedings


Datos del la editorial

Autor: C. Parkinson; N. McAuslane; C. Lumley; S.R. Walker
Título: The Timing of Toxicological Studies to Support Clinical Trials
Editorial: Springer; Springer Netherland
150 Páginas
Año de publicación: 1995-01-31
Dordrecht; NL
Peso: 0,930 kg
Idioma: Inglés
106,99 € (DE)
109,99 € (AT)
118,00 CHF (CH)
POD
XVI, 150 p.

BB; Pharmacology/Toxicology; Hardcover, Softcover / Medizin/Pharmazie; Pharmakologie; Verstehen; clinical trial; efficiency; pharmacology; research; toxicity; Public Health; Pharmacology; Public Health; Public Health und Präventivmedizin; BC; EA

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.

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