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India set for new study on spurious drugs

This article was originally published in SRA

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Executive Summary

India is continuing its efforts to improve its regulatory oversight in the pharmaceutical segment. The country has now initiated steps for a new study on spurious drugs and plans to expand the number of adverse drug reactions (ADR) monitoring centres in the country.

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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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