Breast cancer research and the European Union Clinical Trials Directive

Breast Cancer Research : BCR
Norman Williams

Abstract

Running clinical trials in the commercial sector has always been associated with a certain amount of bureaucracy due to the stringent requirements needed to bring a new drug onto the market. Noncommercial trials have largely been performed outside these requirements. New legislation brought about as a result of the implementation of the European Union Clinical Trials Directive will change this two-tiered approach by harmonizing regulations in all member states. Those who run noncommercial clinical trials will have to find cost-effective ways of dealing with this legislation if such work is to continue in Europe.

References

Nov 21, 2002·European Journal of Cancer : Official Journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR)·Michael BaumMartine Piccart

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Citations

Aug 24, 2010·Clinical Trials : Journal of the Society for Clinical Trials·James D NeatonJens Lundgren
Nov 6, 2018·Current Drug Discovery Technologies·Bhavana B BhatD Sreedhar
Dec 16, 2010·Current Opinion in Critical Care·Katy Robinson, Peter J D Andrews
Nov 18, 2009·PLoS Medicine·Alex D McMahonGordon T McInnes

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