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Sohini Das writes on automobile and healthcare sectors for Business Standard. Over her 17 years as a journalist, she has covered multiple sectors and issues -- FMCG, dairy, tourism, and state elections, among others, across Kolkata, Ahmedabad, and Mumbai. She loves doing personality stories and ground reportage.
Sohini Das writes on automobile and healthcare sectors for Business Standard. Over her 17 years as a journalist, she has covered multiple sectors and issues -- FMCG, dairy, tourism, and state elections, among others, across Kolkata, Ahmedabad, and Mumbai. She loves doing personality stories and ground reportage.
MRP for private market Rs 1,000/ dose; current licence does not allow export or sale in private market
While the Oxford-AstraZeneca vaccine made by Serum Institute here has 70.42% efficacy, Bharat Biotech's still does not have efficacy data as trials are underway in India
India would need 30 million doses in the first phase when it vaccinates the essential services workers including health care professionals, municipal and police staff, etc
US giant Pfizer did not come to present its case on Friday before the Subject Expert Committee
Suresh Jadhav, executive director of the Pune-based firm, said on Friday Serum was seeking approval from the Drug Controller General of India (DCGI) for the two-full dose regimen
Advice comes from Centre; some states begin talks with pharma firms
Most firms plan to increase capacity to meet fresh orders
Bharat Biotech had recently sought an accelerated approval from the regulator based on phase 1 and phase 2 studies
Moderna's vaccine can be stored at normal fridge temperatures of 2 to 8 degrees Celsius for 30 days and it can be stored up to six months at minus 20 degree Celsius, according to reports
Cold chain of agriculture research body may come in handy
If the data is found satisfactory, an approval for Covishield, Oxford-AstraZeneca's vaccine candidate, can come in by the first week of January
At $37 per dose, the Pfizer vaccine is much more expensive compared to $3 per dose for the Covishield
They have the stability data for these investigational products, said a source
The company says they are '200% transparent' about serious adverse events with regulator
The company plans to apply for approval once it finishes phase 3 trials
As it takes away the legal overhang, Cipla can launch the drug once its ANDA is approved
The messenger RNA vaccine candidate contains a short, synthetic version encoding the spike protein (antigen) of the novel coronavirus Sars-CoV-2
DCGI granted conditional approval for phase 1 and 2 clinical trials of Gennova's mRNA based Covid-19 vaccine candidate
Experts ask Bharat Biotech for phase 3 data, Serum's UK approval status
ICMR Director General Balram Bhargava said that in the case of temporary licensure or emergency use, the regulator had to be satisfied with the risk-benefit ratio.