The European Medicines Agency
has published its work programme
for 2014.
Among the priority activities
are the further development
of methods for collecting best
evidence, enhancement of
functionalities of EudraVigilance,
the European database on adverse
drug reactions, the development
of a repository for periodic safety
update reports (PSURs) as well as a
system for monitoring the scientific
literature for signal detection.
EMA will also continue with the
falsified medicines directive that
came into force in 2013.
CLICK HERE for the full program.The above article was sent to subscribers in Pharmacy Daily's issue from 24 Mar 14 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 24 Mar 14
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