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CNN Philippines (Metro Manila) COVID-19 vaccines developed by American pharmaceutical giant Pfizer and its German partner BioNTech, British-Swedish company AstraZeneca, China-based Sinovac, and most recently Russian group Gamaleya Research Institute of Epidemiology and Microbiology obtained emergency use approval from the Food and Drug Administration.
The FDA is still reviewing the applications for emergency use of the coronavirus shot made by India-based Bharat Biotech.
An emergency use authorization is issued for unregistered drugs and vaccines amid a public health emergency, a state which the country is in due to the COVID-19 pandemic. The EUA, which hastens approval for vaccines that normally takes years, is only valid for the duration of the public health emergency declaration, or upon the issuance of a certificate of product registration or CPR. CPR is necessary to sell the drugs and vaccines to the general public.
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