The proposal is part of a wider EU strategy, which also includes
investing around 2 billion euros ($2.3 billion) for the advance
purchase of vaccines under development, in a bid to secure enough
doses for the bloc as it fears lagging behind the United States and
China.
European countries have more stringent rules about research
involving genetically modified organisms (GMOs) than in many other
parts of the world. Reuters already reported last week that the EU's
executive Commission was considering easing those rules for COVID
vaccines.
A Commission document published on Wednesday confirmed the new
proposal. It would reduce member states' power to impose extra
requirements on drugmakers when they conduct clinical trials on
medicines and vaccines containing or consisting of GMOs.
The proposal, which needs to be backed by EU governments and
lawmakers, would be valid only during the COVID-19 emergency.
EU officials said many promising vaccines under development against
the new coronavirus could face delays in European trials if rules
were not relaxed. EU countries now impose extra requirements on
vaccines and drugs containing GMOs, under rules that also cover the
publicly sensitive area of GMO crops.
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In Italy and France, for example, treatments must receive
authorization from government environment or research departments,
as well as from health and drug authorities.
Unless changed, the legal framework would be "likely to cause
significant delay, particularly for multi-center clinical trials in
several member states", the commission document said.
Candidate COVID-19 vaccines are being trailed in several countries
to increase the efficacy of the trials.
The Commission is also proposing laxer rules on language and
packaging requirements for medicines and vaccines to facilitate
their quick distribution during the pandemic.
($1 = 0.8881 euros)
(Reporting by Francesco Guarascio @fraguarascio; Editing by Peter
Graff)
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