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120 mm Issued o n March 14, 2022Version 01| Emergency Preauthorization |COVID-19 Vaccine (Very Cell), Inactivated Please read the leaflet carefully and use the vaccine under the doctor guidanceNAME
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02
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03
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Individuals or organizations seeking to have their product or medication reviewed and approved by the European Medicines Agency
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What is ema starts rolling review?
The EMA starts rolling review is a regulatory procedure used by the European Medicines Agency (EMA) to expedite the assessment of promising new medicines during public health emergencies.
Who is required to file ema starts rolling review?
Pharmaceutical companies that have developed a new medicine and want to get it approved for use in the European Union are required to file for EMA starts rolling review.
How to fill out ema starts rolling review?
Pharmaceutical companies can fill out the EMA starts rolling review application form online on the EMA website and submit all relevant data and information about the new medicine.
What is the purpose of ema starts rolling review?
The purpose of EMA starts rolling review is to speed up the evaluation process of new medicines that are urgently needed to address public health emergencies.
What information must be reported on ema starts rolling review?
Pharmaceutical companies must report data on the safety, efficacy, and quality of the new medicine, as well as information on its manufacturing process and proposed labeling.
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