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US allows use of plasma treatment for COVID patients

The United States health watchdog has given emergency authorisation for the use of blood plasma to treat coronavirus patients in the country, saying the benefits of the treatment outweighed any......

US allows 'game-changer' saliva-based Covid test

The United States health watchdog has authorised the emergency use of a new and expensive saliva based laboratory diagnostic test for COVID-19 that could be a game changer in the diagnosis of the......

Trump defends use of HCQ, says it works in early stages of COVID-19

United States President Donald Trump has again defended the use of hydroxychloroquine to ward off coronavirus, saying many frontline medical workers agree with him that the malaria drug works in......

US withdraws emergency use of hydroxychloroquine for Covid-19

The US food and drug regulatory body on Monday withdrew the emergency use authorisation of anti-malarial drugs chloroquine and hydroxychloroquine in the treatment of COVID-19 patients after......

Anti-malarial drug a 'line of defence' against virus: Trump

United States President Donald Trump on Tuesday defended his taking anti-malarial drug hydroxychloroquine as a 'line of defence' against coronavirus. "I think it's worth it as a line of defence......

Covid-19 could be the boost Indian pharma cos need

The western world had largely considered India to be a production hub, and also, a good potential geography for clinical trials, and a big market. But in Covid-19 research, Indian companies and......

Why train travel will never be the same again

The first two coaches that rolled out from the Railway Coach Factory in Kapurthala also have fixtures coated with titanium dioxide and the provision for plasma air equipment in AC ducts to......

Why Sun Pharma stock will remain under pressure

The weakness in the stock was because of inspections by the American drug regulator at its Halol plant in Gujarat which resulted in eight observations, as well as a downward revision of speciality......

A bitter pill for Aurobindo's sterile drug unit

USFDA issues Form 483 with as many as 14 observations that could impact ongoing operations at Aurobindo's Pashamailaram facility in Hyderabad. A few inspectional observations made by the US......

GSK withdraws sale of Zinetac after health alert

GSK is continuing with investigations into the potential source of the NDMA, which is a known environmental contaminant and found in water and foods, including meats, dairy products, and......

Why Juhi Chawla is waging war against cell phone radiation

'We have created an enemy we can't even see and that enemy is entertaining us while tightening the noose around our necks.''As the radiation increases, it will affect everything -- from your little......

Ferrari wants women drivers for its motor racing academy

IMAGE: Formula One has not had a woman driver start a race since 1976. Photograph: Ferrari/Twitter Ferrari are planning to add female racers to their expanding young driver programme as they seek......

Sports Shorts: MMA's McGregor announces shock retirement

IMAGE: Conor McGregor with belts during a press conference. Photograph: Noah K. Murray-USA TODAY Sports/Reuters Irish mixed martial arts (MMA) fighter Conor McGregor said on Tuesday he was......

Sharapova's intent questioned - Why was she taking banned heart drug?

'Sharapova has been a US resident since early in her career, which does bring in a question of how or why she is using a drug that is not licensed there' IMAGE: Maria Sharapova speaks to the media......
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Maha Govt To Issue Circular For Rational Use Of Remdesivir

Maharashtra Health Minister Rajesh Tope on Friday said the state government will issue circular within 24 hours to all doctors and COVID-19... ...

https://www.news18.com/news/india/maha-govt-to-issue-circular-for-rational-use-of-remdesivir-2908785.html
AstraZeneca still waiting for FDA decision to resume US trial

The US trial of AstraZeneca’s Covid-19 vaccine candidate, initially developed by the University of Oxford, remains on hold while regulators... ...

https://www.hindustantimes.com/world-news/astrazeneca-still-waiting-for-fda-decision-to-resume-us-trial/story-NOIi6zguExvyqmsXbORL6K.html
Samsung gets US FDA nod for ECG app on Galaxy Watches

Thu, Sep 24 2020 10:48:04 AM Seoul, Sep 24 (IANS): Samsung on Thursday said it has received the clearance from the US Food and Drug Administration... ...

https://www.daijiworld.com/news/newsDisplay.aspx?newsID=754339
White House could veto FDA's vaccine rules, says Trump

The Food and Drug Administration is expected to soon issue final guidelines for an emergency-use authorisation. world Updated: Sep 24, 2020 06:45... ...

https://www.hindustantimes.com/world-news/white-house-could-veto-fda-s-vaccine-rules-says-trump/story-3133VQbDWoJFKi29nntSnL.html
Trump says may or may not approve stricter FDA guidelines for Covid vaccine

US President Donald Trump said on Wednesday he may or may not approve any new, more stringent FDA standards for an emergency authorization of a... ...

https://timesofindia.indiatimes.com/world/us/trump-says-may-or-may-not-approve-stricter-fda-guidelines-for-covid-vaccine/articleshow/78286581.cms

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