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Empowering Change: Jubilant Bhartia Foundation and Schwab Foundation for Social Entrepreneurship honours Social Entrepreneur of the Year - India 2024

Over the past fifteen years, the Social Entrepreneur of the Year (SEOY) Award has become one of the most prestigious accolades for social entrepreneurs in ...
Sep 11

Behind the success of every working woman, there are many working women: Neha Dhupia, Beauty Pageant, Model and Bollywood Actress

Fauji kids fare well in beauty pageants may be because of their exposure and better social skills: Neha Dhupia, who won Femina Miss India in ...
Dec 11

TagZ Foods - Shark tank funded snack brand helping people eat healthier

Sagar Bhalotia gives exclusive insights on TagZ Foods which is an Urban Gen Z snack brand. From crafting lip-smacking experiences for consumers to healthier ...
Apr 29

AbCellera-Discovered Antibody, Bebtelovimab, receives FDA Emergency Use Authorization for the treatment COVID-19

Treatment of mild and moderate Covid19 ...
Feb 14

Novavax applies for FDA emergency use authorization of its coronavirus vaccine

Latest Corporate News; Pharma Jan1st/2022...
Feb 01

Meridian Bioscience Receives FDA Emergency Use Authorization for Revogene® SARS-CoV-2 Molecular Assay

Latest news updates...
Nov 12

Covaxin gets EUA for children aged 2-18 years

The Subject Expert Committee (SEC) has approved emergency use of Bharat Biotech's Covaxin for children in the 2-18 years age group...
Oct 12

First needle less COVID vaccines for children and adult above 12 years got approval for EUA

Zydus Cadila’s ZyCov-D, Covid vaccine got Emergency Use Authorization for children and adults 12 years and above ...
Aug 21

GSK and Vir Biotechnology announce joint procurement agreement with European Commission for COVID-19 treatment, Sotrovimab

Latest pharma news update...
Aug 02

FDA issues Actemra drug for COVID under Emergency Use Authorization (EUA)

The drug, Actemra (tocilizumab) has shown efficacy in treating COVID patients with better results by reducing the death and mortality rate along with complications. FDA ...
Jun 25

Roche SARS-CoV-2 molecular test granted first FDA Emergency Use Authorization for PCR testing for Coronavirus

Roche SARS-CoV-2 molecular test for PCR testing is effective for both symptomatic and asymptomatic Covid individuals ...
Jun 22

Merck Announces Supply Agreement with U.S. Government for Molnupiravir

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Jun 09

FDA Emergency Use Authorization Approval for ZEUS ELISA SARS-CoV-2 Total Antibody Test System

Now ELISA bases Covid test from Zeus Scientific...
May 19

FDA Authorizes Pfizer-BioNTech COVID Vaccine for Emergency Use Authorization (EUA) in adolescents for fight against pandemic

FDA is working towards the safety of adolescents and the children who are innocent minds and need special care towards pandemics. FDA authorizes Pfizer-BioNTech ...
May 15

US FDA authorizes Pfizer's Covid-19 vaccine for use in people ages 12 to 15

FDA approves Pfizer vaccine for 12-15 years age group on Monday...
May 11

GSK and Vir Biotechnology starts EMA rolling review of VIR-7831 (sotrovimab) for treatment of COVID-19

GSK's Covid product could be soon in the market after the emergency medical application review...
May 11

Emergency Use Authorization of a new drug for the treatment of COVID19

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May 10

Remdesivir – Antiviral drug for treatment of COVID 19

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Apr 24

The need and importance of Emergency Use Authorization (EUA) by FDA (Food and Drug Administration)

Of all industries, the pharmaceutical and healthcare industry has got a major boost from this pandemic. All the efforts are going out to the development ...
Apr 20

US may not use AstraZeneca vaccine , Dr Anthony Fauci

WHO found that a causal relationship between the vaccines and blood clotting events is considered plausible but is not confirmed...
Apr 10

Ongoing trial shows Pfizer Covid-19 vaccine remains highly effective after six months

Latest data proves Pfizer BioNTech vaccine to have long lasting effect...
Apr 02

GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19

The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ...
Mar 27

GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19

The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ...
Mar 27

J&J vaccine is only 66% effective in global trial though company claims 85% efficacy for severe cases

Johnson and Johnson vaccine may not be efficient as others but may prove to be of use due to raging pandemic and shortage of standard ...
Jan 30

Pfizer and BioNTech reach agreement with COVAX for advance purchase of Vaccine to Help Combat COVID-19

Initial agreement provides up to 40 million doses to COVAX in 2021 ...
Jan 23

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