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India vows to decide on foreign vaccines within 3 days to fast-track imports

    Published: 15 Apr 2021 06:20 PM BdST Updated: 15 Apr 2021 06:20 PM BdST Workers from Afghan health ministry unload boxes containing vials of COVISHIELD, a coronavirus disease (COVID-19) vaccine donated by Indian government in Kabul, Afghanistan February 7, 2021. REUTERS/Omar Sobhani/File Photo India said on Friday its drugs regulator will decide on emergency-use applications for foreign COVID-19 vaccines within three working days from application, as it tries to attract Pfizer, Johnson ...
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Just 3 days! India cuts approval time for foreign Covid-19 vaccines

Just 3 days! India cuts approval time for foreign Covid-19 vaccines India will provide approvals to COVID-19 vaccines approved by health regulators like US FDA within 3 days; detailled guidelines to come soon Joe C Mathew | April 15, 2021 | Updated 15:05 IST India will take only three working days to clear the applications to import and supply 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). The countrys d...
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Health ministry issues regulatory pathways for foreign-produced Covid-19 vaccines | India News

NEW DELHI: 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. The Central Drugs Standards Control Organisation (CDSCO) headed by Drugs Controller General of India (DCGI) has explained that it prepare detailed guidelines specifying regulatory pathway for approval of foreign approved Covid vaccines ba...
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Govt issues regulatory pathway for Covid-19 foreign vaccines approved for restricted use

Regulatory pathway for foreign vaccines issued April 15, 2021 CDSCO will widely disseminate these guidelines to the concerned stakeholders The government, on Thursday, issued regulatory pathway related to 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). The Central Drugs Standards Control Organisation (CDSCO), headed by Drugs Controller General of India or DCGI, has laid out the pathway according to which ...
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Health Ministry issues regulatory pathways for foreign-produced COVID-19 vaccines

Health Ministry issues regulatory pathways for foreign-produced COVID-19 vaccines ANI | Updated: Apr 15, 2021 14:35 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. The Central Drugs Standards Control Organisation (CDSCO) h...
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Source: aninews.in

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To grant EUA to foreign vaccines, DCGI will take decision in 3 working days

Amid record spike in daily coronavirus infections, Indias drug regulator will take a decision on applications seeking approval for restricted emergency use of foreign produced vaccineswithin three working days from the date of submission, the government said on Thursday. The CentralDrug Authority, CDSCO, will process applications for registration certificates (registration of overseas manufacturing site and product; in this case COVID vaccine) and import license within three working days from...
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Health Ministry issues regulatory steps to approve foreign made COVID-19 vaccines

Health Ministry issues regulatory steps to approve foreign made COVID-19 vaccines Health Ministry issues regulatory steps to approve foreign made COVID-19 vaccines 15 April 2021 | News DCGI will consider and take a decision within three working days from the date of submission of the complete application Image credit- shutterstock.com The Union Health Ministry has issued the Regulatory Pathway in India for COVID-19 Vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Jap...
United Kingdom Union Health Ministry National Covid National Expert Group On Vaccine Administration Vaccination Programme Regulatory Pathway

Indian regulator to decide on foreign vaccine makers' applications in 3 days : The Tribune India

1144 Aditi Tandon New Delhi, April 15 Amid a COVID spike and daily cases setting a new grim peak on Thursday, the Indian drug regulator said that it would process the applications from the makers of the already approved COVID vaccine.  The process would take place within three working days of submission of fast track job procurement and fast track process.     Detailing the regulatory pathway that would enable foreign-made vaccines to enter the Indian markets, the Central Drug Standards Con...
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Alert: Whatsapp Can be Briefly Suspended by an Attacker Due to Vulnerability Detected

Alert: Whatsapp Can be Briefly Suspended by an Attacker Due to Vulnerability Detected A vulnerability, which can allow an attacker to suspend your Whatsapp acount for a brief period of time by using your phone number, has been recently detected.   |  13 April 2021 9:15 AM GMT NEW DELHI: Security experts have found a flaw in the popular instant messaging app WhatsApp, where an attacker can temporarily suspend your WhatsApp account by simply using your phone number. Due to fundamental weakness...
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US: Large crowds at WrestleMania 37 in Tampa

Tampa, United States – Handmade banners, foam fingers and roars of rage and rapture. All that and more finally returned to World Wrestling Entertainment (WWE) as the company hosted its first large crowd in more than a year, and did so at its biggest show – WrestleMania. “I have personally missed the interaction with the audience tremendously,” said Paul Heyman, the on-screen manager of WWE Universal Champion Roman Reigns. “There’s a level of passion of WWE fans that I would dare sug...
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