"us-regulators"

Following today's positive advisory committee meeting outcome regarding the Janssen Biotech Inc. Covid-19 Vaccine, the US Food and Drug Administration has informed the sponsor that it will rapidly work toward finalisation

The Moderna approval comes exactly a week after the US Food and Drug Administration okayed a shot from Pfizer and its German partner BioNTech.

Pfizer said the vaccine had no serious side effects and that the company will apply for emergency use authorization from US regulators "within days"