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'Promising but not perfect': generics industry's take on EMA's literature monitoring service

This article was originally published in SRA

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Executive Summary

Generics companies have several reservations about the European Medicines Agency's new literature monitoring service, under which the agency intends to check several reference databases and journals for suspected adverse reactions involving 400 active substances1-3.

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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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