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    3038 Hennepin Ave Minneapolis, MN
    612-822-4611

Open Daily: 10am - 10pm | Alley-side Pickup: 10am - 7pm
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The Timing of Toxicological Studies to Support Clinical Trials

The Timing of Toxicological Studies to Support Clinical Trials

Parkinson, C.
McAuslane, N.
Lumley, C.

Hardcover

Medical Reference

ISBN10: 0792388720
ISBN13: 9780792388722
Publisher: Springer Nature
Published: Jan 31 1995
Pages: 150
Weight: 0.92
Height: 0.44 Width: 6.14 Depth: 9.21
Language: English
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.

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