New Delhi [India], March 31 (ANI): Meeting of Subject Expert Committee (SEC) of the Central Drugs Standard Control Organisation (CDSCO) will be held on Wednesday to deliberate on emergency use authorisation application of Russian vaccine Sputnik V.
Cambridge [UK], March 22 (ANI): AstraZeneca said on Monday that the company plans to apply for emergency use authorization from the US Food and Drug Administration for its Covid-19 vaccine in the first half of April.
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/
Geneva [Switzerland], March 13 (ANI): The World Health Organization (WHO) on Friday issued emergency use authorization for Johnson & Johnson's coronavirus vaccine, paving the way for the one-shot dose to be used as part of the United Nation's international vaccine distribution effort.
Washington DC [US], March 10 (ANI): 340 different coronavirus tests have so far won emergency use authorisation (EUA), including one that can be used at home without a prescription to detect the virus, the Food and Drug Administration (FDA) has said.
Washington [US], March 1 (ANI): US' Centers for Disease Control and Prevention (CDC) advisory committee on Sunday has voted to recommend that Johnson & Johnson's COVID-19 vaccine can be given to people ages 18 and older in the United States.
Washinton [US], February 28 (ANI): The United States authorised Johnson & Johnson's COVID-19 vaccine for emergency use on Saturday, adding a third vaccine to the US arsenal to fight the pandemic as the death toll due to the infection crosses 5.11 lakh.
New Delhi [India], February 24 (ANI): The Central Drugs Standard Control Organisation's (CDSCO) Subject Expert Committee (SEC) has recommended additional immunogenicity data from Dr Reddy's Laboratories which applied to the national drugs regulator seeking emergency use approval for Sputnik
Washington [US], February 24 (ANI): The US Food and Drug Administration said on Wednesday that Johnson and Johnson's single-dose COVID-19 vaccine has met the requirements for emergency use authorisation.
New Delhi [India], February 24 (ANI): The Central Drugs Standard Control Organisation's (CDSCO) Subject Expert Committee (SEC) is going to meet on Wednesday afternoon to discuss Dr Reddy's Laboratories application seeking emergency use approval (EUA) for SputnikV, a Russian Vaccine.
Hyderabad (Telangana) [India], Feb 19 (ANI): Dr Reddy's Laboratories said on Friday it has initiated the process with the Drugs Controller General of India (DCGI) for emergency use authorisation of human adenoviral vector-based platform vaccine candidate Sputnik V.