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World Health Organization (WHO) defines pharmacovigilance as âthe science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drugrelated problemâ. Once a drug is released in the market by FDA, it is monitored for its safety profile. Further, the adverse effects caused by the drug are reported to generate post-marketing surveillance data. Lipika Chablani, Pharmacovigilance of Biosimilars.

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Last date updated on June, 2014

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