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Clinical Trials Safety Regulation

UK MHRA Finds Labs Releasing Unreliable Data Due To Pressure From Pharma

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Executive Summary

A UK regulator with the MHRA is concerned that bioanalytical laboratories are not being given enough time to do their job properly by drug companies under pressure to ensure their clinical trials remain on schedule. 

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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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