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GMP Guidance For Phase I IND Trials Will Benefit Drug Manufacturers, Labs

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Executive Summary

Manufacturers and laboratories producing investigational new drugs in Phase I studies are exempt from having to fully validate their manufacturing process under new FDA guidelines

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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