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BioPharmaceutical Europe Regulation

Europe's IT Roadmap Will Support Clinical Trials Reg, New Medicines Portal

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Executive Summary

Sweeping initiative to upgrade and standardize IT systems across Europe's drug regulatory network will also support enhanced pharmacovigilance and centralized applications process.

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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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