New Delhi [India], September 18 (ANI): World Health Organisation's (WHO) approval for the emergency use authorisation (EUA) to COVID-19 vaccine Covaxin, developed by the Hyderabad-based Bharat Biotech, is likely to be delayed till October 5.
New Delhi [India], July 27 (ANI): Ahmedabad-based Zydus Cadila has submitted additional data related to immunogenicity and safety, on its three-dose COVID-19 vaccine ZyCoV-D, to India's drug regulator Drugs Controller General of India (DCGI), sources said on Tuesday.
New Delhi [India], July 15 (ANI): The Drug Controller General of India (DCGI) has urged Pfizer, Johnson and Johnson twice in writing to apply for emergency use authorisation for their COVID-19 vaccine so that application is processed well in time but pharma companies have not applied for
New Delhi [India], July 12 (ANI): India's drug regulator Drugs Controller General of India (DCGI) will consider giving emergency use authorisation (EUA) to Zydus Cadila for its COVID-19 vaccine ZyCoV-D in a few more days, sources told ANI.
New Delhi [India], July 1 (ANI): The pharmaceutical firm Zydus Cadila on Thursday informed that it has applied for emergency use authorisation (EUA) from the Drug Controller General of India (DCGI) for its DNA vaccine ZyCoV-D against coronavirus disease and stated that they expect to produce
New Delhi [India], July 1 (ANI): Pharmaceutical major Zydus Cadila on Thursday applied for Emergency Use Authorisation (EUA) seeking approval from the Drugs Controller General of India (DCGI) for the launch of their ZyCoV-D vaccine for 12 years and above, sources said .
New Delhi [India], June 18 (ANI): Pharmaceutical major Zydus Cadila has told the Centre that it could apply for emergency use authorisation (EUA) for ZyCoV-D vaccine in the next seven-eight days.
New Delhi [India], June 10 (ANI): The Director General of Health Services (DGHC) under the Union Health Ministry on Wednesday issued guidelines for the management of COVID-19 in children below 18 years of age, according to which use of Remdesivir, an emergency use authorisation drug, has
Hyderabad (Telangana) [India], June 1 (ANI): Biological E. Limited has tied up with Canada's Providence Therapeutics to locally manufacture its mRNA coronavirus disease (COVID-19) vaccine, the Hyderabad-based company announced on Tuesday, adding it will run a pivotal trial in India, and seek
Geneva [Switzerland], May 1 (ANI): The World Health Organization (WHO) on Friday listed the Moderna coronavirus vaccine for emergency use, adding another shot to its arsenal in the fight against the coronavirus.
New Delhi [India], April 14 (ANI): Congress leader Rahul Gandhi on Wednesday took a jibe at the central government after it granted permission for emergency use authorisation of Sputnik-V, the Russian vaccine against COVID-19.
New Delhi [India], April 13 (ANI): Union Health Minister Dr Harsh Vardhan on Tuesday accepted that Russia's Sputnik V vaccine against coronavirus has got the emergency use authorisation, making it the third vaccine apart from Covishield and Covaxin to be used in India.