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AstraZeneca is the only vaccine for the prevention of COVID-19 that has been signed by the government. However, news that the vaccine could be difficult to obtain FDA approval from the US Food and Drug Administration this year raised concerns that national introduction could hamper it. The government said it is unlikely and stressed that there will be no changes to the security plan for the first half of next year. This is reporter Hyungwon Lee. Even if the US Food and Drug Administration delays approval of the AstraZeneca vaccine, the government’s position is that it will not have a significant impact on the domestic market. If there are no serious side effects, it is believed that it will pass, but the approval or not and the national introduction are independent. The Ministry of Food and Pharmaceutical Safety decides whether it should be used in Korea, and one of the factors to consider is whether or not the developing country of the vaccine should approve it. The experts noted that the possible delay in FDA approval appears to be a combination of American interests and should be approached with caution. This is not a problem of side effects, but the fact that there is no difference in efficacy or clinical results over 55 years is not a serious defect. Meanwhile, it was confirmed that President Trump’s executive order for preferential vaccination for nationals was not related to obtaining domestic vaccines. The government emphasized that the goal of introducing AstraZeneca in the first half of next year will remain unchanged, as it has already agreed that AstraZeneca’s domestic production volume will be supplied first. YTN Hyungwon Lee[[email protected]]it is. ※ ‘Your report becomes news’ YTN is waiting for your valuable report.
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