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USFDA

Merck and Ridgeback seek EUA from USFDA for Molnupiravir

Merck and Ridgeback Biotherapeutics yesterday announced that Merck has submitted an Emergency Use Authorisation (EUA) application to the US Food and Drug...
DCGI CDSCO

DCGI grants EUA to Truenat for Nipah virus tests in India

New Delhi: Truenat is the first kit in India to receive Emergency Use Authorization (EUA) by the DCGI for conducting Nipah virus tests. It is a point of...
DCGI CDSCO

DCGI grants EUA to Hetero’s Biosimilar Version of Tocilizumab

India, Hyderabad: Hetero announced today that the Drug Controller General of India (DCGI) has issued for restricted use, Emergency Use Authorization (EUA)...
CDSCO DCGI FDA

NATCO applies to CDSCO for EUA of Molnupiravir capsules

Natco Pharma has applied to the Central Drugs Standard Control Organization (CDSCO) in India for approval of Phase-III clinical trial of Molnupiravir...
Meeting Committee FDA

CDSCO experts to meet again on Jan 1 on EUA for vaccine

The Subject Expert Committee (SEC) in the Central Drugs Standard Control Organisation (CDSCO) has decided to reconvene tomorrow, January 1 (Friday) after...
Medicine Injection Doctor

Bharat Biotech seeks EUA for Covaxin

After Pfizer and Serum Institute, Bharat Biotech applied to the central drug regulator seeking emergency use authorisation for its C-19 vaccine Covaxin,...
Medicine Vaccine

Serum Institute applies for EUA for vaccine in India

The Serum Institute of India has applied to the Drugs Controller General of India (DCGI) seeking emergency use authorisation for the Oxford...
Justice Court

Eli Lilly files litigation against 20 Indian Pharma Companies

The US drug major Eli Lilly is fighting a patent infringement litigation against several Indian pharma companies for the intellectual property rights...
Sun Pharma

Sun Pharma to introduce Molnupiravir in India

Sun Pharma recently said that it is gearing up to introduce Merck Sharpe Dohme (MSD) and Ridgeback’s Molnupiravir under the brand name...
Zudus

Zydus Cadila’s vaccine to be administered to adults only as of now

New Delhi: Zydus Cadila’s C-19 vaccine, ZyCov-D, which has been cleared by India’s drug regulator for those aged 12 years and above, will...
WHO

Novavax, Serum Institute seek approval from WHO for Covid-19 vaccine

NEW DELHI: Biotechnology firm Novavax Inc said it has completed the rolling submission for the emergency use listing (EUL) of its Covid-19 vaccine candidate...
Ad Marketing

These Indian Pharma Cos seek nod from DCGI for marketing Anti Covid drug Molnupiravir

Hyderabad-based Natco Pharma Limited and Hetero have sought marketing authorisation for their anti-Covid drug molnupiravir from the drug regulator, people in the know told ET. The Subject...
Laboratory

EU Regulator starts real-time review of anti viral drug Molnupiravir

Merck said today that the European Union’s (EU) drug regulator has initiated a real-time review of its experimental C-19 antiviral drug for...
USFDA

USFDA approval for J&J and Moderna C-19 booster dose

The US Food and Drug Administration (USFDA) has amended the emergency use authorisations (EUAs) for the Johnson & Johnson and Moderna C-19...
USFDA

USFDA advisers to review Merck’s Molnupiravir soon

A panel of outside advisers to the US health regulator will meet late next month to discuss whether to authorise Merck &...
Injection vaccine Medicine

Biological E seeks DCGI nod for Phase-III trial of Corbevax

Biological E has sought permission from India’s drug regulator to conduct the phase-III clinical trial for its C-19 vaccine Corbevax as a...
Medicine Injection Vaccine

USFDA Staff: Moderna did not meet all criteria for booster dose

Scientists at the U.S. Food and Drug Administration (USFDA) said on Tuesday that Moderna Inc had not met all of the agency's criteria to support use...
Pharmacy, Medical Store

KSRP urges Govt and PCI to amend admission process to the Diploma in Pharmacy

BENGALURU: The Karnataka State Registered Pharmacists’ Organisation has written to PM Narendra Modi, Union Health Minister Mansukh Mandaviya, Minister of State for...
NPPA Price of drugs

NPPA releases proposed retail price calculation for 7 formulations

The National Pharmaceutical Pricing Authority (NPPA) has released the price calculation sheet of proposed retail price of seven drug formulations including for...

FDA की टीम ने मेडिकल स्टोर पर की छापेमारी, मेडिकल सील: Haryana

FDA की टीम ने मेडिकल स्टोर पर की छापेमारी Haryana: Bahadurgarh शहर के सैनीपुरा में स्थित मेडिकल स्टोर...
DCGI CDSCO

Bharat Biotech awaits DCGI nod to launch Covaxin for children

After getting approval from the Subject Expert Committee (SEC) for Covaxin to be used for children in the two-to-18 years of age...
Air Cargo Import Export

Govt allows export of Sputnik Light made in India

The government has permitted the export of Russia’s single-dose C-19 vaccine Sputnik Light domestically produced here as the jab has not yet...
DCGI CDSCO

Aurobindo Pharma, MSN Labs seek DCGI nod for Phase-III trials of Molnupiravir

Two Indian pharmaceutical companies have sought permission from India’s drug regulator to continue phase III trials on antiviral drug molnupiravir in mild C-19 patient....
WHO

WHO to give approval to Covaxin soon: Health Experts

The decision on Bharat Biotech's C-19 vaccine, Covaxin Emergency Use Listing (EUL) by the World Health Organisation (WHO) is expected in October, informed the top health experts in...

Latest posts

High Court restrains publishing Ads in a dispute on Chyawanprash

The Calcutta High Court has issued an interim injunction restraining Shree Baidyanath Ayurved Bhawan Pvt Ltd from issuing certain print and video...

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