A book on Pharmacovigilance is a valuable resource for anyone involved in the healthcare pharmaceutical or regulatory sectors. It plays a crucial role in understanding drug safety by focusing on identifying evaluating and preventing adverse drug reactions (ADRs). Such a book provides in-depth knowledge about monitoring drug safety and ensuring public health. It also helps professionals navigate the regulatory framework for pharmacovigilance offering guidance on compliance with national and international guidelines such as ICH FDA EMA and WHO standards.
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