New legislation on pharmacovigilance for medicinal products for human use: information for healthcare professionals and patients

The new European legislation, which aims at strengthening and rationalizing pharmacovigilance for medicinal products for human use, came into force in July 2012 in the European Union. In this context a number of texts about some concepts of pharmacovigilance are available.

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Contact: vig@afmps.be


 

 

 

 

 

 

 

 

 

 

 

Last updated on
17/09/2012