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tezlivenews · 2 years
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भारत बायोटेक की Covaxin को मान्यता देगा ब्रिटेन, जानिए भारत के लिए क्यों है गुड न्यूज?
भारत बायोटेक की Covaxin को मान्यता देगा ब्रिटेन, जानिए भारत के लिए क्यों है गुड न्यूज?
हाइलाइट्स भारत बायोटेक की कोवैक्सीन को मान्यता देगा ब्रिटेन 22 नवंबर से कोवैक्सीन लगवाए लोगों को क्वारंटीन नहीं करेगा ब्रिटेन कोविशील्ड को पहले ही मंजूरी दे चुका है ब्रिटेन, भारत के लिए खुशखबरी लंदनब्रिटिश सरकार भारत बायोटेक की कोवैक्सीन को मान्यता देने जा रही है। इस वैक्सीन को विश्व स्वास्थ्य संगठन ने कुछ दिनों पहले ही अपनी स्वीकृति दी थी। 22 नवंबर को कोवैक्सीन ब्रिटेन के अंतरराष्ट्रीय…
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harpianews · 3 years
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Vaccinated but stuck: Indians await WHO's nod for homegrown shot to travel abroad
Vaccinated but stuck: Indians await WHO’s nod for homegrown shot to travel abroad
Stranded for nine months in a village in southern India and unable to return to his job in Saudi Arabia, Sugathan PR is hoping the World Health Organization will approve the Indian COVID-19 shot Covaxin, paving the way for his journey. Like Sugathan, millions of Indians have taken Covaxin and many have complained of travel conflicts as the vaccine is not recognized for international travel by…
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mykrantisamay · 2 years
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कोवाक्सिन को डब्ल्यूएचओ से मंजूरी: वैक्सीन सर्टिफिकेट से लेकर प्रतिबंध तक, जानें भारतीयों को कितना होगा फायदा?
कोवाक्सिन को डब्ल्यूएचओ से मंजूरी: वैक्सीन सर्टिफिकेट से लेकर प्रतिबंध तक, जानें भारतीयों को कितना होगा फायदा?
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technomoz · 2 years
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WHO panel likely to decide on Covaxin EUL today; here’s what you need to know
WHO panel likely to decide on Covaxin EUL today; here’s what you need to know
The World Health Organization’s Technical Advisory Group for Emergency Use List (TAG-EUL) is likely to list Bharat Biotech’s COVID-19 vaccine after some additional clarification from Bharat Biotech and a final assessment of risks and benefits on Wednesday. “The Technical Advisory Group for the Emergency Use List (TAG-EUL) is an independent advisory group that makes recommendations to the WHO on…
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kwttoday · 3 years
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India : Delay in WHO's approval of Covaxin
India : Delay in WHO’s approval of Covaxin
India : Delay in WHO’s approval of Covaxin India’s Bharat Biotech has been submitting data on the EUL of Covaxin “regularly and very quickly” to a technical committee which hopes to have a final recommendation to the WHO next week, a top official of the global health agency said, stressing that the UN body “trusts” the Indian industry that manufactures high quality vaccines. The Supreme Court…
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dainikviral · 3 years
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We trust Indian industry, Bharat Biotech has been submitting data regularly, very quickly: WHO official on Covaxin EUL
We trust Indian industry, Bharat Biotech has been submitting data regularly, very quickly: WHO official on Covaxin EUL
India’s Bharat Biotech has been submitting data on the EUL of Covaxin regularly and very quickly to a technical committee which hopes to have a final recommendation to the WHO next week, a top official of the global health agency said on Thursday, stressing that the UN body “trusts” the Indian industry that manufactures high-quality vaccines. Hyderabad-based Bharat Biotech, which has developed…
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doonitedin · 3 years
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Health Minister Mandaviya, WHO chief Tedros hold 'detailed iteraction' over Covaxin's emergency use listing
Health Minister Mandaviya, WHO chief Tedros hold ‘detailed iteraction’ over Covaxin’s emergency use listing
Image Source : TWITTER/WHO CHIEF Health Minister Mandaviya, WHO chief Tedros hold ‘detailed iteraction’ over Covaxin’s emergency use listing  In a telephonic conversation with Health Minister Mansukh Mandaviya, World Health Organisation Chief Tedros Adhanom Ghebreyesus on Tuesday discussed the emergency use listing of Bharat Biotech’s Covaxin. The resumption of supplies of the Serum Institute of…
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collapsedsquid · 3 years
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India's regulators gave the vaccine an emergency approval in January while the third phase of the trial was still under way, sparking scepticism and questions from experts.
Bharat Biotech, the vaccine's manufacturer, said the latest findings were "an important milestone in vaccine discovery, for science and our fight against coronavirus".
"With today's results from our phase 3 clinical trials, we have now reported data on our Covid-19 vaccine from phase 1, 2, and 3 trials involving around 27,000 participants," the firm said.
The drug regulator has also given the green light to the Oxford-AstraZeneca vaccine, known as Covishield in India, to be used.
The country launched its vaccine drive, the world's largest inoculation effort, in early January. It has vaccinated nearly 30 million people so far - healthcare and frontline workers were given priority in the first phase. People over 60 and those who are between 45 and 59 but have other illnesses are now getting vaccinated.
The government aims to cover 250 million "priority people" by the end of July. But experts say that the pace of vaccination has been slow and unless the drive is scaled up, the target could be missed.
India is also supplying the vaccine to neighbouring countries and a host of other nations. It has shipped tens of thousands of free doses of Covid-19 vaccines to several countries in what is being widely described as "vaccine diplomacy".
The country is a vaccine powerhouse: it makes 60% of the world's vaccines and is home to half a dozen major manufacturers.
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reportodisha · 2 years
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Centre Clears Two More Vaccines And Anti-Viral Drug Molnupiravir For Emergency Use
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December 28
Center Approves Molnupiravir For Emergency Use
Central Drugs Standard Control Organisation on Tuesday approved two more coronavirus vaccines and one anti-viral drug for emergency use in India. The two latest vaccines cleared by India are Corbevax and Covovax. The anti-viral drug Molnupiravir can be used during emergency. Union Health Minister Dr Mansukh Mandaviya said in a tweet, Further strengthening the fight against COVID-19, CDSCO, has given 3 approvals in a single day for: - CORBEVAX vaccine - COVOVAX vaccine - Anti-viral drug Molnupiravir for restricted use in emergency situation. Corbevax is made by the Hyderabad-based firm Biological-E. "It's a hat-trick! It's now third vaccine developed in India," Mr Mandaviya said. The other two vaccines developed in India are Bharat Biotech's Covaxin and the Serum Institute of India's (SII) Covishield. Also, Health Minister said, the anti-viral drug Molnupiravir will be manufactured in India by 13 companies for restricted use under emergency situation to treat adult patients with COVID-19 and who have high risk of progression of the disease. So far, eight COVID-19 vaccines have got emergency use authorisation from India's drug regulator. Those are Covishield, Covaxin, ZyCoV-D, Sputnik V, Moderna, Johnson and Johnson, Corbevax and Covovax. Click here for more news....   Read the full article
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tezlivenews · 3 years
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WHO अगले हफ्ते देगा भारत बायोटेक की कोवैक्सिन पर फैसला, मंजूरी के लिए पूरी करनी होंगी कुछ शर्तें
WHO अगले हफ्ते देगा भारत बायोटेक की कोवैक्सिन पर फैसला, मंजूरी के लिए पूरी करनी होंगी कुछ शर्तें
जिनेवाभारत-बायोटेक की कोवैक्सिन को लेकर विश्व स्वास्थ्य संगठन (WHO) का फैसला अगले हफ्ते आने वाला है। WHO ने बताया है कि एक्सपर्ट्स के एक स्वतंत्र समूह के साथ मिलकर अगले हफ्ते एक बैठक की जाएगी और इस बात पर फैसला किया जाएगा कि कोवैक्सिन को इमर्जेंसी में इस्तेमाल के लिए मंजूरी देनी है या नहीं।WHO ने ट्वीट कर बताया कि कोवैक्सिन निर्माता Bharat Biotech विश्व स्वास्थ्य संगठन को कुछ-कुछ समय पर…
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harpianews · 2 years
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Finally, WHO approves India's homemade Covaxin for global use; Facilitates overseas travel and exports
Finally, WHO approves India’s homemade Covaxin for global use; Facilitates overseas travel and exports
The World Health Organization (WHO) on Wednesday provided the Emergency Use List (EUL) for Covaxin, a COVID-19 vaccine developed by the Indian Council of Medical Research (ICMR) and Hyderabad-based Bharat Biotech. The WHO’s decision implies that the indigenously developed Covaxin meets the standards set by it for protection against corona virus disease. It also largely removes the uncertainty…
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rvpgmedia · 2 years
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If Covaxin is awaiting WHO approval, here is a list of countries where it has been deleted | Latest News India
https://rvpgmedia.com/?p=66347 If Covaxin is awaiting WHO approval, here is a list of countries where it has been deleted | Latest News India https://rvpgmedia.com/?p=66347...
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pgurus · 2 years
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Given the amazing success of COVAXIN in treating COVID variants — why are the US and the West not giving emergency approval?
The disapproval of United States of America towards the emergency use authorization (EUA) to Covaxin, manufactured by an Indian company, Bharat Biotech is creating an unwanted doubt in the minds of the people. The decision of by the American government was conveyed to the American partner, Ocugen even before the manufacturers submitted a EUA application for the Covaxin.
The United States country is in no longer a situation where it requires to fast forward the approvals of Covid-19 vaccines to increase the supplies for immunization of their citizens. According to Bio Tech, India, the United States government has already invested approximately $18 billion in the development of various vaccines like Pfizer-BioNTech, Moderna-NIAIDmRNA and Johnson and Johnson’s Vector jabs. With these developments in 2020, the country has managed to vaccinate a considerate number of population to achieve a good herd of immunity.
In the current scenario, the United States Food and Drugs Administration has decided on a new strategy to prioritize their reviews of EUA requests on the basis of clinical trials, the integrity of the trial data, and whether the manufacturing facilities for the inactivated whole virus vaccine meet appropriate standards as set by the United States government.
With the ongoing process of review and prioritization, the US FDA has recommended Ocugen to now apply for a full authorization for the vaccine instead on an emergency approval. For the approval Bharat BIoTech needs to provide more informational data from clinical trials to be well assured that Covaxin is safe, prompts immune response among the vaccinated citizens and has an acceptable efficacy.
However this process is expected to take approximately a year to get the approval for Covaxin to be used in the United States.
There have been doubts arising in the minds of people around the world who are vaccinated with Covaxin if they will be allowed to travel to United States if they are vaccinated with Bharat BioTech’s Covaxin. As a matter of fact, if you are not restricted from travelling to the United States in the current situation, it clearly signifies that the country requires a negative RT-PCR test for the travelers to be able to board a flight.
Probably if a student is looking forward to attend a university in the United States in the fall, it is unlikely that having received two doses of Covaxin will stop you from being able to enter the country. As Covaxin has still not received any approval from the US government. Several universities have allowed international students to “restart” their immunization upon arrival in the US with one of the approved vaccines that are available in the country.
The vaccine is still going to be reviewed by the US FDA under a standard approval process that may take time. In the meantime, Bharat Biotech has also submitted an application for an Emergency Use License from the World Health Organization, which it expects will come between July and September this year.
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kwttoday · 3 years
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WHO waiting on more information from Bharat Biotech before approving Covaxin
WHO waiting on more information from Bharat Biotech before approving Covaxin
WHO waiting on more information from Bharat Biotech before approving Covaxin On Monday, The World Health Organisation said that it was waiting for additional data from Bharat Biotech on its Covid Vaccine called Covaxin, which is under examination by experts of WHO for approval of Emergency Use Listing. “Who has been working closely with Bharat Biotech. The technical advisory group will meet on…
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updatesnews · 2 years
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UK changes travel rules on vaccination and travel for under 18s in new announcement | Travel News | Travel
UK changes travel rules on vaccination and travel for under 18s in new announcement | Travel News | Travel
The latest Government update said: “From 4am on Monday 22 November, the Government will recognise vaccines on the World Health Organisation’s Emergency Use Listing (WHO EUL) at our border. “In practice, this means that Sinovac, Sinopharm Beijing and Covaxin will be added to our list of approved vaccines for inbound travel, benefitting more fully vaccinated people from countries around the…
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doonitedin · 3 years
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Bharat Biotech's Covaxin to get WHO nod this week, say sources
Bharat Biotech’s Covaxin to get WHO nod this week, say sources
Image Source : PTI/FILE Bharat Biotech’s Covaxin to get WHO nod this week, say sources Bharat Biotech’s Covaxin will get approval from the World Health Organisation (WHO) this week, sources told news agency ANI. The government had informed Parliament in July that it has submitted all documents required for Emergency Use Listing (EUL). WHO usually takes up to six weeks to decide on Emergency Use…
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