Hardcover. Zustand: Fine. New York/London/Australia/Canada/New Zealand: A ROC Book/Penguin Group, 1991. Unread. Book shows light age, light extremity wear still FINE, Dust Jacket (see scan), light extremity age, just a touch of wear, otherwise Fine. BCE, Original ISBN : 0451450795. Book Club Edition. Hard Cover/Cloth Spine/Sewn. Fine/Near Fine. 8vo - 8 " tall.
Sprache: Englisch
Verlag: Kluwer Academic Publishers, 1994
ISBN 10: 0792388720 ISBN 13: 9780792388722
Anbieter: Fireside Bookshop, Stroud, GLOS, Vereinigtes Königreich
Verbandsmitglied: PBFA
EUR 17,84
Anzahl: 1 verfügbar
In den WarenkorbCloth/Laminated Boards. Zustand: Very Good. Type: Book 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 harmonization. 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 has brought together representatives of the pharmaceutical industry from Europe, Japan and the USA to give a comprehensive account of current international industry positions on the subject. The contributions in this text review the situation and address the clinical and strategic requirements of the pre-clinical 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. Small mark at base of spine.128pp.