Search For "authorisation"
SEC recommends authorisation to Covaxin without 'clinical trial mode'
Updated : 5 years ago IST
New Delhi [India], March 10 (ANI): The Subject expert committee (SEC) of Drugs Controller General of India (DCGI) on Wednesday recommended removing the "clinical trial mode" condition related to Bharat Biotech's Covaxin.
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340 different COVID-19 tests approved so far in US
Updated : 5 years ago IST
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.
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US FDA panel gives go-ahead to Johnson & Johnson's COVID-19 vaccine
Updated : 5 years ago IST
Washington [US], February 27 (ANI): A US Food and Drug Administration (FDA) advisory panel on Friday endorsed Johnson & Johnson's coronavirus vaccine and recommended the agency grant emergency authorisation.
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Johnson & Johnson's single-dose COVID-19 vaccine meets requirements fo
Updated : 5 years ago IST
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.
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Dr Reddy's initiates process for emergency use authorisation of Sputnik V
Updated : 5 years, 1 month ago IST
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.
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Pfizer showed no plans to generate safety data in Indian population for CO
Updated : 5 years, 1 month ago IST
New Delhi [India] February 5 (ANI): The subject expert panel of Drugs Controller General of India did not recommend granting emergency use authorisation to Pfizer's COVID-19 vaccine noting that the firm has not proposed plans to generate safety and immunogenicity data concerning Indian popu
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Enzene Biosciences Ltd. obtains marketing authorization for its first bios
Updated : 5 years, 1 month ago IST
Pune (Maharashtra) [India], February 4 (ANI/PRNewswire): Recently Enzene Biosciences Ltd. announced that it has obtained Marketing Authorisation (MA) from Drug Controller General of India (DCGI) for Teriparatide - bioactive part of human parathyroid hormone (PTH), an anabolic approach to the
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EU authorises AstraZeneca COVID-19 vaccine
Updated : 5 years, 1 month ago IST
Brussels [Belgium], January 30 (ANI): The European Commission on Friday granted a conditional marketing authorisation (CMA) for the COVID-19 vaccine developed by multinational pharmaceutical company AstraZeneca.
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Covishield, Covaxin are safest of COVID-19 vaccines, side-effects are neg
Updated : 5 years, 2 months ago IST
New Delhi [India], January 12 (ANI): Covishield and Covaxin, the two COVID-19 vaccines which have received Emergency Use Authorisation (EAU) have been tested on thousands of people and side-effects are negligible, Dr VK Paul, Member (Health), NITI Aayog, said on Tuesday and noted that the
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COVID-19 vaccine may cost between Rs 200 to 295 in India: Health Ministry
Updated : 5 years, 2 months ago IST
New Delhi [India], January 12 (ANI): Union Health Secretary Rajesh Bhushan on Tuesday said the COVID-19 vaccine may cost in the range of Rs 200 to 295 in India and two vaccines -- Covishield and Covaxin -- have received Emergency Use Authorisation (EAU) after going through established saf
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Bolivia registers Sputnik V vaccine for emergency use authorisation
Updated : 5 years, 2 months ago IST
Moscow [Russia], January 7 (ANI): The Russian Direct Investment Fund (RDIF) on Wednesday announced that Bolivia's State Agency for Medicines and Health Technologies has registered Sputnik V Covid-19 vaccine under emergency use authorisation procedure.
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India prepared to roll out COVID-19 vaccine within 10 days of emergency us
Updated : 5 years, 2 months ago IST
New Delhi [India], January 5 (ANI): Days after Drugs Controller General of India (DCGI) gave approval to two COVID-19 vaccines, Union Health Secretary Rajesh Bhushan on Tuesday said that India is prepared to roll out vaccine within 10 days of emergency use authorisation (EUA), subject to
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