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The Timing of Toxicological Studies to Support Clinical Trials (Hardcover, 1994 ed.): C. Parkinson, N. McAuslane, C. Lumley,... The Timing of Toxicological Studies to Support Clinical Trials (Hardcover, 1994 ed.)
C. Parkinson, N. McAuslane, C. Lumley, S.R. Walker
R2,882 Discovery Miles 28 820 Ships in 10 - 15 working days

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 objective of these Workshops has been to provide an international forum for regula tory, academic and industry representatives to debate together, and suggest solutions to, specific problems. The meeting reported in this volume represents a departure from this approach, in that the par ticipants were drawn largely from the pharmaceutical industry. Senior clinicians, pharmacologists and toxicologists from companies in Europe, the USA and Japan met in May 1994 to discuss a scientific rationale for the conduct of toxicity studies to support the clinical development of new medicines, and to begin to work towards an industry consensus. Achievement of such a consensus is seen as an important step in the process leading towards international harmon isation of the recommendations on the timing of toxicity studies in relation to clinical trials."

The Timing of Toxicological Studies to Support Clinical Trials (Paperback, Softcover reprint of the original 1st ed. 1994): C.... The Timing of Toxicological Studies to Support Clinical Trials (Paperback, Softcover reprint of the original 1st ed. 1994)
C. Parkinson, N. McAuslane, C. Lumley, S.R. Walker
R2,753 Discovery Miles 27 530 Ships in 10 - 15 working days

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 objective of these Workshops has been to provide an international forum for regula tory, academic and industry representatives to debate together, and suggest solutions to, specific problems. The meeting reported in this volume represents a departure from this approach, in that the par ticipants were drawn largely from the pharmaceutical industry. Senior clinicians, pharmacologists and toxicologists from companies in Europe, the USA and Japan met in May 1994 to discuss a scientific rationale for the conduct of toxicity studies to support the clinical development of new medicines, and to begin to work towards an industry consensus. Achievement of such a consensus is seen as an important step in the process leading towards international harmon isation of the recommendations on the timing of toxicity studies in relation to clinical trials."

Wild Flowers of the Undercliff, Isle of Wight (1881) (Paperback): Charlotte O'Brien, C. Parkinson Wild Flowers of the Undercliff, Isle of Wight (1881) (Paperback)
Charlotte O'Brien, C. Parkinson
R636 Discovery Miles 6 360 Ships in 10 - 15 working days

This scarce antiquarian book is a selection from Kessinger Publishing's Legacy Reprint Series. Due to its age, it may contain imperfections such as marks, notations, marginalia and flawed pages. Because we believe this work is culturally important, we have made it available as part of our commitment to protecting, preserving, and promoting the world's literature. Kessinger Publishing is the place to find hundreds of thousands of rare and hard-to-find books with something of interest for everyone!

Wild Flowers Of The Undercliff, Isle Of Wight (1881) (Paperback): Charlotte O'Brien, C. Parkinson Wild Flowers Of The Undercliff, Isle Of Wight (1881) (Paperback)
Charlotte O'Brien, C. Parkinson
R570 Discovery Miles 5 700 Ships in 10 - 15 working days
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