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Vaccines available or that will be available in the European Union must meet EU approval and quality standards, but there may be limited exceptions that allow member states to market temporarily unauthorized emergency products, a spokesman for the EU said on Friday. European Comission. .
Stefan De Keersmaecker In response to a question at a press conference in Brussels, the Member State applying it is responsible for marketing a vaccine without EU authorization.
He stressed that safety was a priority for the European Commission and that it was therefore of the utmost importance that no medicine was placed on the market in the European Union without a marketing authorization based on a full evaluation under EU law. .
It is also very important that citizens have reliable information on vaccine safety, which is why the European Medicines Agency (EMA) is constantly evaluating and monitoring these vaccines, he said. As soon as a vaccine is available, the European Commission will launch it implementing an EU vaccination strategy, he added.
In response to a question from a spokesperson, the spokesperson replied that Péter Szijjártó Russia said it would start shipping small quantities of its coronavirus vaccine to Hungary in December so they could inspect the vaccine and complete the final steps in the licensing process. Tamás Menczer, Hungary’s State Secretary for Information and International Presentation at the Ministry of Foreign Affairs and Foreign Affairs also said Thursday that Hungary may also receive a vaccine sample from a Chinese manufacturer for analysis.
Featured image: Georgiy Zimarev / Sputnik / AFP
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