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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...
DCGI CDSCO

DCGI’s nod to AstraZeneca to import, market Selumetinib Capsules

NEW DELHI: Drug firm AstraZeneca Pharma India on Sunday said it has received import and market permission from the Indian drug regulator Drugs Controller General India (DCGI) for...
Job

Govt Job for M.Pharm, M.Sc as Scientist at WHO

World Health Organisation (WHO) is the directing and coordinating authority for health within the United Nations system. It is responsible for providing...
WHO

WHO emergency use authorisation to Covaxin delayed till October 5

New Delhi : World Health Organisation's (WHO) approval for the emergency use authorisation (EUA) to C-19 vaccine Covaxin, developed by the Hyderabad-based Bharat Biotech,...
USFDA

Zydus Cadila gets tentative nod from USFDA for Brexpiprazole tablets

Zydus Cadila has received tentative approval from the US Food and Drug Administration (USFDA) to market Brexpiprazole tablets in the strength of...
ICMR

Single vaccine shot 96.6% effective: ICMR

New Delhi: A single dose of any Covid vaccine is 96.6 per cent effective in preventing mortality, while with two doses the effectiveness...
PCI

PCI asks institutions to start B Pharm (Practice) Course

Download PCI circular dated 07-09-2021: The Pharmacy Council of India (PCI) has directed the affiliated institutions, which are conducting B Pharm courses,...
NABL

NABL releases NABL 136: specific criteria for X-Ray equipment

Download NABL 136: The National Accreditation Board for Testing and Calibration Laboratories (NABL) has released NABL 136: specific criteria for accreditation of...
USFDA

USFDA to review use of Blood Disorder Therapy in children

Global Blood Therapeutics Inc said on Tuesday the U.S. Food and Drug Administration (USFDA) had granted priority review for two applications related to its treatment...

B-Hub: Biopharma Hub to come up at Hyderabad’s Genome Valley

HYDERABAD: With the objective of imparting impetus to biopharmaceutical research and manufacturing in the country, the Telangana government is developing a B-Hub.
Govt of India

Govt may impose anti dumping duty on import of vitamin C from China

The Union finance ministry is likely to impose an anti-dumping duty on vitamin C imported from China to provide a level playing...

Pfizer becomes first Covid vaccine globally to get full USFDA approval

American drug regulator, the US Food and Drug Administration (USFDA), on Monday granted full approval to the Pfizer vaccine for the prevention...

Here are some facts about Zydus Cadila’s Vaccine ZyCoV-D

Here are some facts about Zydus Cadila's Vaccine ZyCoV-D A day after getting the emergency use authorisation (EUA) in...

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