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The Federal Food and Drug Administration of the United States (FDA for its seals in English) has made a minor change to allow you to have one large impact on the authorization that the Modern laboratory has to distribute its vehicle against the COVID 19.
Hasta ahora Moderna has distributed its vaccine in cases containing 10 doses each. The new FDA decision indicates that the laboratory can stop 15 doses per week. If so, with the ability to distribute in the country, it can transport a 50 per cent more dose, accelerating the distribution of this vaccine throughout the country.
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This change will take place to watch in the next week, meanwhile new packages will be delivered from today. But including antes is going to be another change. With the existing material in each of the existing visas, the FDA authorized to release 11 doses by way of 10. From the start, hospitals and pharmacies will be alerted as to the materials of Modern sober material for the vaccine. The ever-increasing problem is finding the relevant water for extra strength. The FDA has approved the authorization for the dose available at the evacuation centers.
“These revisions are subject to Moderna’s authorization having a positive impact on the distribution of doses. I have more vacancies available in our communities, which will allow more doses to be added to the braces of our most fast-growing people, ”said a FDA-appointed vacancy regulator, Peter Marks. “In the last instance, when more vacancies are added to the fast-paced population, we will speed up the end of the pandemic ”.
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The other large FDA-authorized exchange for Modern, is that the vacuum can be maintained at a good ambient temperature for 24 hours, and only 12 hours as indicated at this time. And once the life is over, it can be maintained in good conditions for 12 hours and not for 6 hours, as long as the norm is high.
The vacuum cleaner is transported to low temperatures, but one time The vials are available at the evacuation center, now they have all one day to be rescued. The idea is to avoid taking doses that are not used.
Since February the laboratory has been in Conversations for realizing these changes in its authorization, however, require the FDA to complete a period of investigation and testing prior to approval.
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“We are committed to learn and increase constantly to facilitate the administration of our vacancy against COVID 19, which simplifies the work of the medical staff and accelerates the immunization programs ”, declared in a communication Stéphane Bancel, President of Modern.
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