Pfizer’s COVID-19 Pill Receives FDA Authorization

Pfizer’s COVID-19 treatment, Paxlovid, has received emergency use authorization (EUA) by the FDA. The drug, which can be taken orally in the form of a pill, is authorized for the treatment of mild-to-moderate COVID-19 in adults and pediatric patients over 12. Eligible patients need to have a positive COVID-19 test and be at high risk for progression to severe COVID-19, including hospitalization or death. Paxlovid is available by prescription only and is recommended to be started as soon as possible after diagnosis of COVID-19 and within five days of symptom onset.

Benjamin Franklin Institute of Technology and Ginkgo to Create Biomanufacturing Associates Degree

The Benjamin Franklin Institute of Technology (BFIT) partnered with Ginkgo Bioworks to develop an associate degree in biotechnology manufacturing. The program will be housed at the Nubian Square Life Science Training Center, a collaboration of organizations working to meet the demand for a well-trained and diverse life sciences workforce, with additional funding through a $100,000 grant from Kargman Family Foundation.

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