What type of vaccine is it? How was it made/what are the components? When was it tested? Where is it being used? When was it approved for use by governments?

The CoronaVac vaccine, developed by Sinovac Biotech and Tianjin Institute of Biological Products Co. Ltd., is a inactivated virus vaccine that utilizes an inactivated version of the SARS-CoV-2 virus to produce immunity against Covid-19. The vaccine consists of whole killed viruses which are then combined with immunologic adjuvants (chemicals) to increase the body’s sensitivity and response to the antigen once injected into the body. This type of vaccine has proven successful at preventing other viral diseases such as polio, hepatitis, influenza and others.

CoronaVac was first tested in early 2020 on animals, including monkeys and mice. In July 2020, Phase I/II human trials were conducted in three cities across China involving 910 volunteers aged 18-59 years old. No significant adverse reactions were reported during those trials; however minor side effects such as pain at injection site or fever were experienced by some participants. After successfully passing these trials, it began Phase III clinical testing in August 2020 with more than 30,000 volunteers from Brazil and Indonesia participating in mid to late stage clinical trials. By November 10th 2020 Phase III results have been announced proving CoronaVac to be effective at preventing Covid-19 infection with an efficacy rate 86%.

Background information on the CoronaVac(Sinovac) Covid-19  vaccine: What type of vaccine is it? How was it made/what are the components? When was it tested? Where is it being used? When was it approved for use by governments?

As of December 28th 2020 CoronaVac has begun being used for mass vaccinations across China after receiving approval from the Chinese government for use on humans by December 6th 2020 following completion of its phase 3 clinical trial results released earlier that same month . It also has received emergency use authorization from Turkey due to high demand for a safe coronavirus vaccine when compared with alternatives available elsewhere like Pfizer’s mRNA technology which requires ultra low temperatures for storage and transportation making it difficult to transport short distances within Turkey given their existing infrastructure limitations.. On February 4th 2021 Brazil approved emergency use authorization allowing millions of doses already produced there locally since June last year become available for public vaccination programs throughout Latin America where Sinovac had recently signed agreements with several countries looking purchasing large quantities of vaccines including Argentina Peru Colombia Chile etcetera while still awaiting approval from more affluent countries like Australia United States Canada Japan Korea amongst others..

Overall Sinovac’s corona Vaccine is one successfully approved and now being used globally that provide protection against Covid 19 infection using traditional safe methods that have been successful time over time even though they may not provide 100% total protection they certainly help reduce numbers infected significantly thereby helping flatten out curves health care systems worldwide can handle without becoming overwhelmed leading towards eventual herd immunity through multiple approaches rather than just relying solely on newer mRNA technologies alone . As such this helps promote equitable access vaccination around world especially poorer nations unable acquire other alternatives due cost or technological transfer restrictions imposed wealthier countries control intellectual property rights thus enabling them gain most benefit market value wise over less affluent ones unable afford higher purchase prices …

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