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    Vietnam to Receive 2 Lakh COVAXIN from Bharat Biotech as Donation

    The Republic of Vietnam will receive 2,00,000 doses of Bharat Biotech COVAXIN®. Dr. Krishna Ella, Chairman and Managing Director of Bharat Biotech revealed this at a function hosted by H.E Mr. Vuong Dinh Hue, President of the National Assembly of the Socialist Republic of Vietnam in the presence of distinguished dignitaries in New Delhi today.

    This represents a gesture of goodwill to provide access to Bharat Biotech WHO-approved, indigenously developed COVAXIN® to fight the COVID19 Pandemic across borders. COVAXIN® has received EUL in Vietnam.

    Bharat Biotech was invited by the Embassy of Vietnam for a one-on-one meeting with H.E the President of the National Assembly, to discuss avenues of cooperation, supplies, and technology transfer possibilities.

    Dr. Krishna Ella Chairman and Managing Director of Bharat Biotech said, “We believe in vaccine equity, global public health, and having access to the vaccine is vital for national health, and I hope everyone in the Republic of Vietnam will take advantage of having access to the widely administered, safe and efficacious COVAXIN®.”

    In Vietnam, Bharat Biotech has been working with Duc Minh Medical JSC, towards the commercialization of INDIRAB (Inactivated Rabies Vaccine). Duc Minh is Bharat Biotech’s local partner in Vietnam.

    Bharat Biotech has also supplied INDIRAB® to the Republic Nation supporting their national rabies vaccine requirement

    Bharat Biotech and Duc Minh donate 2 lakh covaxin doses to Vietnam

    Ms. Suchitra Ella, Joint Managing Director of Bharat Biotech expressed, it is an honour for us to serve the Republic of Vietnam humbly and wish COVAXIN® contribution will help boost up the country’s national vaccination program and recovery from the pandemic. We also like to thank H.E of Vietnam for inviting us to meet and discuss opportunities for collaboration.”

    Bharat Biotech has completed Phase-2 and Phase-3 trials of COVAXIN® for children in the age group 2 to 18 years. The data has been submitted to the Central Drugs Standard Control Organisation (CDSCO) and the final approval is awaited. On approval, children will also have access to COVAXIN®.

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