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Within a week, AstraZeneca will deliver the vaccine approval documentation (Oxford) to regulatory agencies. This was stated by Piero Di Lorenzo, president and CEO of Irbm Pomezia, who collaborates in the development, guest of the program “The entrepreneur and the others” on Cusano Italia Tv. “The parent company AstraZeneca is preparing all the documentation, the entire package from deliver to regulatory agencies – Di Lorenzo explained -. I trust that this package will be ready and delivered within a week ”.
In the meantime, before the end of the year, the green light for Pfizer doses could arrive. The European Medicines Agency has received an application for conditional marketing authorization of the vaccine developed by BioNTech and Pfizer. This was announced by the EMA. The evaluation will proceed on an accelerated schedule. An opinion on the authorization could arrive within a few weeks. If the data presented are sufficiently robust to draw conclusions on the quality, safety and efficacy of the vaccine, EMA’s Scientific Committee for Medicinal Products for Human Use (CHMP) will conclude its assessment at an extraordinary meeting scheduled for 29 December, at the latest. late.
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