FDA sets up task force to fast track registration of Covid-19 meds

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FDA sets up task force to fast track registration of Covid-19 meds
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The Food and Drug Administration (FDA) has formed a task force to hasten and streamline the approval and evaluation of medicines for Covid-19.

The Food and Drug Administration has formed a task force to hasten and streamline the approval and evaluation of medicines for Covid-19.

This also “seeks to streamline the approval and evaluation of Covid-19 drugs without compromising efficacy, quality, and safety,” he said. “Now, with the introduction of Taskforce Fleming, Covid-19 drugs that will be approved and issued with Certificates of Product Registration will be readily-accessible to the general public in FDA-licensed drug establishments,” he noted.

There are currently two Covid-19 drugs with approved CPR by the FDA—-these are ronapreve and remdesivir, the Department of Health said.

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