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Guidance Documents

Pharmacovigilance is the process of monitoring the use of medicines in practice to identify previously unrecognised adverse events or changes in the patterns of known adverse events. These include both user safety and consumer safety. The guidelines below are links to the various bodies and only adopted guidelines are included. If you want additional information (such as Concept Papers, Draft Guidelines, comments etc.) please visit the websites.

Last Updated: 26 June 2012

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