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Pfizer May Apply For Emergency Use Of Covid 19 Vaccine By Late November Fox Business Man Eating Apple Stock Image
Man eating apple stock image. As we get closer to an important data readout from our covid 19 vaccine program i wanted to speak directly to the billions of people millions of businesses and hundreds of governments around the world that are investing their hopes in a safe and effective covid 19 vaccine to overcome this pandemic. I cannot think of a breakthrough that would be more meaningful to a greater number of people than an effective and safe covid 19 vaccine the open letter reads. Pfizer ceo albert bourla wrote an open letter stating it was likely the vaccine would if it works and is safe be submitted to the us food and drug administration in the third week of november.
Ceo albert bourlas letter says the earliest the company could apply for authorization for its covid 19 vaccine is the third week of november. Pfizer had said previously that. Pfizer targets emergency approval next month says ceo in an open letter.
One of the companies hard at work on developing a vaccine for covid 19 is pfizer. All nine ceos signed the following pledge. Pfizers greek ceo open letter about a covid 19 vaccine.
In an open letter pfizer chairman and ceo albert bourla said while millions of population and the governments globally were investing their hopes in a safe and effective covid 19 vaccine to overcome the pandemic he would like to clarify about development timelines. That milestone should be achieved in the third week of november pfizer chief executive officer albert bourla said in an open letter published friday on the companys website. The ceos of astrazeneca biontech glaxosmithkline johnson johnson merck moderna novavax pfizer and sanofi have made a historic pledge to the world outlining a united commitment to uphold the integrity of the scientific process as they work towards potential regulatory filings and approvals of the first covid 19 vaccines.
2 min read. The covid 19 vaccine bnt162b2 is also in a rolling review with the european medicines agency.
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