| 英文摘要 |
The world is still during a Corona virus disease 2019 (COVID-19) pandemic. As world health organization (WHO) and countries around the world to work together on the response by tracking the pandemic, advising on critical interventions, distributing vital medical supplies to those in need, they are racing to develop and deploy safe and effective vaccines. However, several pharmaceutical companies have developed successfully the safe and effective vaccines that prevent people from getting seriously ill or dying from COVID-19, such as AstraZeneca, Johnson & Johnson, Moderna and Pfizer-BioNTech. All these world regulatory organization recognized vaccines were under the agreement to use by the emergency use authorization (EUA). More importantly, Taiwan biotech company Medigen Vaccine Biologic corp. also announced their MVC-COV1901 for preventing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which permitted by Taiwan 1st EUA authorization this year. Thus, our study aims to discuss about the deference between the different vaccines according to the of their research and design (R&D) technologies. Another issue we address is about the regulation of drug development and usage of EUA between Unite Sates and Taiwan. The results of our argument might provide the insight of technologies of COVID-19 vaccine and information for medical practitioner or people who are medical professional, such as pharmacist, registered nurse or medical technologist. |