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Under an emergency use regulation hundreds of thousands of people in china have been given chinese vaccines before final regulatory approval for general use.

Vaccine vial monitor slideshare. Zheng zhongwei head of chinas covid 19 vaccine development task force and an official at the national health commission said the emergency use which is in accordance with the chinese vaccine management law allows vaccine candidates to be used for a limited period of time among certain people at high risk of contracting the disease such as medical workers front line pandemic control workers and customs workers. The head of the us food and drug administration thursday said the agency would consider an emergency use authorization to expedite getting a vaccine against the coronavirus strain covid 19 to. Food and drug administration recently increased some requirements for granting an emergency use authorization eua for a covid 19 vaccine but serious deficiencies remain sidney wolfe founder of public citizens health research group said in testimony thursday before the agencys vaccines and related biological products advisory committee.

Boxes of sars cov 2 vaccine for covid 19 stamped with the words state authorized emergency use produced by sinovac are stacked at its factory in beijing on thursday sept. Trial kits for the pfizer covid 19 vaccination study reuters sign up for our special edition newsletter to get a daily update on the coronavirus pandemic. Hundreds of thousands of people have already taken experimental covid 19 vaccines in china since it launched its emergency use programme in july aimed at essential workers and other limited groups.

Abdulrahman bin mohammed al owais said that the vaccine has been authorised for emergency use as part of the countrys measures to protect health workers in close contact with covid 19 patients and ensure their safety and that it was fully aligned with the regulations and laws that allow a faster review of licensing procedures. Drugmaker pfizer said tuesday that it plans to apply for emergency use authorization from the food and drug administration for its covid 19 vaccine in november once safety milestones are achieved. Usually market approval from a regulatory agency like the us fda is needed to use a vaccine in the community.

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