Textbook Of Pharmacovigilance Icri Institute Of Clinical Research

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Pharmacovigilance—an umbrella term used to describe the processes for monitoring and evaluating ADRs—is a key component of effective drug regulation systems, clinical practice and public health programs. The principal concern of pharmacovigilance is the detection of ADRs in real world clinical trial that are novel by virtue of their clinical nature, severity and/or frequency as soon as possible with minimum patient exposure. The scope of pharmacovigilance needs to be extended beyond the strict confines of detecting new signals of safety concerns. Globalization, consumerism and the resulting explosion in free trade and communication across borders and increasing use of the internet have all changed the way medicinal products and information about them is accessed. These changing patterns in drug use require a shift in the approach to pharmacovigilance. The system and the key players in the field have to be geared up to be more closely linked and more responsive towards the management of the ADRs. This book Textbook of Pharmacovigilance has been the concentrated effort to compile all the theoretical and practical aspects of pharmacovigilance, for easy accessibility to any new entrant in the field and serve as a ready reference for those actively involved in the area. The book introduces basic definitions, classifications, objectives and elaborates the practical aspects including setting up of pharmacovigilance center, regulations in various countries, data mining, risk-benefit assessment, etc. It also provides latest updates on key issues like pharmacogenetics and herbal drug monitoring

Height949 mm
Length8 mm
Width724 mm
Weight163 g
Language TypePublished
Number Of Pages440
Package Quantity10
Product GroupBook
Publication Date2011-04-22
PublisherJaypee Brothers Medical Publishers
StudioJaypee Brothers Medical Publishers
Sales Rank7609

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