New legislation on pharmacovigilance for medicinal products for human use: information for marketing authorisation holders

The new European legislation, which aims at strengthening and rationalizing EU pharmacovigilance for medicinal products for human use, came into force in July 2012 in the European Union. "Pharmacovigilance - New legislation”, which is accessible via the homepage of the famhp website, gives relevant documents for marketing authorisation holders for medicinal products for human use.

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Contact : vig@afmps.be

 

 

 

 

 

 

 

 

 

 

 

 

Last updated on
18/09/2012