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Health Ministry issues regulatory pathways for foreign-produced COVID-19 v
Updated : 4 years, 11 months ago IST
New Delhi [India], April 15 (ANI): The Central Government on Thursday issued the regulatory pathway in India for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency Use Listing (EUL), said the Union Health Ministry.
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DFC to support Indian manufacturer Biological E's efforts to produce 1 bil
Updated : 5 years ago IST
Washington [US] March 13 (ANI): The US International Development Finance Corporation (DFC) has announced it will support Indian manufacturer Biological E's efforts to produce at least 1 billion doses of COVID-19 vaccines by the end of 2022 with stringent regulatory authorization (SRA) and/
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