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Top 30 Pharma and Biotech Companies in 2023: Statistics and Trends

XTalks

Paxlovid was first authorized under the FDA Emergency Use Authorization in December 2021 ; however, it has received FDA approval on May 25, 2023. pneumoniae serotypes) replaced the company’s first pneumococcal conjugate vaccine Prevnar (PCV7, approved by the FDA in February 2000) in a February 2010 FDA approval.

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2020 Year in Review: COVID-19, CRISPR and Immunotherapies Define the Year for the Life Sciences

XTalks

However, now, test results can be delivered within a day or two thanks to better coordination, ramped up production of test supplies as well as development of rapid tests. Omer maintains that the solution to this challenge is something that’s already in practice by developers of the mRNA vaccines. Vaccine Considerations.