The drug regulatory body of India, DCGI is waiting for the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) approval to AstraZeneca & Oxford’s COVID19 Vaccine, before giving a nod for Emergency Use Authorisation to its Indian counterpart developed by Serum Institute of India (SII) . It’s expected for British- Sweden giant drugmaker AstraZeneca in the UK to get authorization at any time, Sources to The Medically Speaking team
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