EXPLAINER: The whos and hows in the process of Covid vaccine approval

After the DOST-VEP and SJERB review the application, it will then be submitted to the Food and Drugs Administration , which grants the Certificate of Product Registration for a vaccine.to issue an emergency use authorization to Covid-19 vaccines.from six months to 21 days.

“Tinitignan nila at sinisigurado na walang personal, salungat na interest, o conflict na interest na pumapasok sa proseso. Tinitignan nila kung sino ‘yung bumoboto tungkol sa positive recommendation, walang stock holder sa manufacturer, walang merong political interest,” the doctor explained. The first group consists of the activities under the research and development for the Covid-19 vaccines. Meanwhile, the second group is focused on the tasks of the core agencies in connection with the work results of the first group.The vaccine approval starts with the three phases of clinical trials. As explained by Dans, in Phase 1, few volunteers are given jabs of the vaccine to see if there are any significant effects.

However, Dans explained that the country is in an emergency due to many deaths and active Covid-19 cases. “Sa sitwasyon na ito, meron tayong preliminary data. ‘Di pa po tapos yung data, kailangan na nating magdesisyon kung aling bakuna ang gagamitin.”

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