Now, the Drugs Controller General of India DCGI will consider this recommendation and decide whether to grant Sputnik V approval for restricted emergency use in India
Analysts at Phillip Capital believe that it is not over for the Indian pharma - and that it is all set for a sectoral value upgrade
Dr Reddy's Laboratories on Wednesday announced termination of Avigan trial study being conducted in Kuwait
Stock market updates: Nifty PSU Bank index surged over 6 per cent and was the top sectoral gainer
The teams were from Gennova Biopharmaceuticals Ltd in Pune, Biological E Ltd and Dr Reddys Laboratories Ltd in Hyderabad.
A PMO release said three vaccines are in advanced stages of development in India, out of which two are in Phase II and one is in Phase-III
A short-covering move, along with addition of fresh position, is seen only if somehow Nifty sustains level of 11,200
The next upside for Nifty Pharma is located above the resistance of 12,100 levels.
Upon regulatory approval in India, RDIF shall supply to Dr. Reddy's 100 million doses of the vaccine
The ongoing pace of product launches in the US should lead to stronger growth after a good Q1, say analysts
The drug is a therapeutic equivalent generic version of Zytiga owned by Johnson & Johnson
Under new terms, DRL to hold back Rs 300 crore and release it if the revenue from sale of the products forming part of the business undertaking during the 12 months post-closing exceeds Rs 480 cr
The USFDA has recently given an emergency approval to the drug for use on coronavirus patients
The company said, with this, all facilities under warning letter are now determined as Voluntary Action Indicated (VAI)
Local pharma units have already started work on developing patented drugs, some have already approached regulator for approvals
Patient groups urge govt to revoke Gilead's remedesivir patent in the wake of the crisis
It's the therapeutic generic equivalent of Geodon Injections
Earlier, the drug major had said that the US health regulator has issued a Form 483 with two observations after inspecting the facility but later it was issued revised Form 483 with one observation
21,026 votes, which accounted for the rest 0.02 per cent, were posted against the resolution, it added
First Indian firm to get contract for supplying generic schizophrenia drug to public hospitals there