ISBN: 9789401114240
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ISBN: 9789401114240
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ISBN: 9789401114240
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ISBN: 9789401114240
Over the past twelve years, the Centre for Medicines Research has held a series of Workshops on a number of topics related to the drug discovery and development process.The major objectiv… Plus…
C. Lumley; N. McAuslane; C. Parkinson; S.R. Walker:
Timing of Toxicological Studies to Support Clinical Trials - nouveau livre2012, ISBN: 9789401114240
eBooks, eBook Download (PDF), Over the past twelve years, the Centre for Medicines Research has held a series of Workshops on a number of topics related to the drug discovery and developm… Plus…
ISBN: 9789401114240
Over the past twelve years, the Centre for Medicines Research has held a series of Workshops on a number of topics related to the drug discovery and development process. The major objecti… Plus…
ISBN: 9789401114240
*The Timing of Toxicological Studies to Support Clinical Trials* / pdf eBook für 96.49 € / Aus dem Bereich: eBooks, Fachthemen & Wissenschaft, Medizin Medien > Bücher nein eBook als pdf e… Plus…
2012, ISBN: 9789401114240
eBooks, eBook Download (PDF), [PU: Springer Netherlands], Springer Netherlands, 2012
Données bibliographiques du meilleur livre correspondant
Informations détaillées sur le livre - The Timing of Toxicological Studies to Support Clinical Trials
EAN (ISBN-13): 9789401114240
Date de parution: 2012
Editeur: Springer Netherlands
Livre dans la base de données depuis 2017-01-19T21:05:31+01:00 (Paris)
Page de détail modifiée en dernier sur 2023-08-12T05:41:43+02:00 (Paris)
ISBN/EAN: 9789401114240
ISBN - Autres types d'écriture:
978-94-011-1424-0
Autres types d'écriture et termes associés:
Auteur du livre: parkinson, tim walker, lumley
Titre du livre: clinical trials
Données de l'éditeur
Auteur: C. Parkinson; N. McAuslane; C. Lumley; S.R. Walker
Titre: The Timing of Toxicological Studies to Support Clinical Trials
Editeur: Springer; Springer Netherland
150 Pages
Date de parution: 2012-12-06
Dordrecht; NL
Langue: Anglais
96,29 € (DE)
99,00 € (AT)
118,00 CHF (CH)
Available
XVI, 150 p.
EA; E107; eBook; Nonbooks, PBS / Medizin/Pharmazie; Pharmakologie; Verstehen; clinical trial; efficiency; pharmacology; research; toxicity; C; Pharmacology/Toxicology; Public Health; Pharmacology; Public Health; Biomedical and Life Sciences; Public Health und Präventivmedizin; BB
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.Autres livres qui pourraient ressembler au livre recherché:
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