Vaccination related to the COVID-19 pandemic turned out to be a global experiment. In the absence of clinical studies for assessing safety, dosage, immune response of subjects of different age groups, etc., vaccination as a means of reducing the number of victims practically replaced the final phase of the customary cycle of trials for FDA approval. Given this reality, methods for post-hoc evaluation need to be designed. This would serve as guidance for future preventive measures.
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Published on: Nov 22, 2024 Pages: 54-56
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DOI: 10.17352/asb.000024
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