Why is it necessary
to allow enough time for medicines agencies to evaluate new medicines?
Leaflet 1
Why is it necessary
to regularly re-evaluate the benefits and risks of medicines? Leaflet 2
Why should access
to independent information on the risks of medicines be guaranteed?
Leaflet 3
Why use the
INN (International Nonprorietary Name) rather than the brand name
of a medicine? Leaflet 4
Why can the
centralised procedure for
marketing authorisations be extended without negative consequence
for national medicines agencies? Leaflet 5
Why can't pharmaceutical
firms convey any other information than promotional stuff? Leaflet 6
Why is real
therapeutic innovation so rare? Leaflet 7
Why must there
be a European regulatory framework to guarantee "compassionate
use" of medicines in terminally ill patients? Leaflet 8
Why should the
length of data protection for medicines not be extended? Leaflet 9
Why is it important
to have access to documents of the European Medicines Evaluation
Agency (EMEA)? Leaflet 10
Why is it necessary
to switch the European Medicines Evaluation Agency (EMEA) to the
Directorate General of the European Commission responsible for health
and consumer protection? Leaflet 11
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