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Meeting Committee FDA

Expert Committee on FDCs calls for information from stakeholders

The expert committee, constituted by the Union health ministry for examining the permission of licenses for 19 fixed dose combinations (FDCs) approved...
Meeting Committee FDA

DCGI to constitute expert committee for regulation of new drugs, INDs

The Drugs Controller General of India (DCGI) is planning to constitute one or more expert committee or...
Pharmacy, Medical Store

Dedicated chapter on Medical Devices should be included in Pharmacy Course: Experts

Faculty experts in pharmaceutical sciences and regulatory officers are of the view that study of medical devices should be made a mandatory...
Medicine Factory

Fermentation products mfg may need more push than PLI scheme: Experts

Even as the Central government has come out with significant measures to support production of key starting materials (KSMs), active pharmaceutical ingredients...
CDSCO DCGI FDA

Lupin gets CDSCO committee nod for marketing Ranibizumab

Lupin Ltd has received marketing approval from the Subject Expert Committee (SEC) at Central Drugs Standard Control Organisation (CDSCO) for Ranibizumab.
Medicine

Bring Nutraceuticals for prevention of diseases under DCGI’s regulation: Experts to Govt

Regulatory oversight and lack of clarity on upper tolerable limit (UTL) and recommended dietary allowance (RDA) standards have prompted manufacturers across the...
Meeting Committee FDA

Guidelines on post-approval changes in drugs: Sub-committee DCGI

The sub-committee, constituted by the Drugs Controller General of India (DCGI), has submitted the guidelines on post-approval changes in drugs to the...
Bp Apparatus, Medical Devices

Govt needs to make India self-reliant in Medical Devices: Experts

Experts are stressing that the state and central governments must give a big push to the Research and Development (R&D) for the...
Nasal drops Medicine

Nasal vaccine gets nod for Phase 1 trial from CDSCO’s expert panel

CDSCO’s expert panel recommended granting permission for conducting phase 1 clinical trial of an intranasal vaccine against C-19 developed by Bharat Biotech,...
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...
CDSCO DCGI FDA

CDSCO expert panel to review vaccine applications today

NEW DELHI : An expert committee of the Central Drugs Standard Control Organisation (CDSCO) will meet today to review applications of Pfizer, Serum Institute...
Meeting Committee FDA

Committee to identify investment opportunities, bottlenecks in pharma industry: DoP

Committee to identify investment opportunities, bottlenecks in pharma industry The Department of Pharmaceuticals (DoP) has created a six-member expert...
Justice Court

Constitute Committee To Boost Indian Pharma Sector: Madras HC

The Madras High Court's Justice N Kirubakaran has said that India has emerged as a pioneer in pharmaceuticals. Yet, for the basic...
Document

FDA & PCB offices should be within Pharma Parks for speedy approvals: Experts

Experts in the industry are of the opinion that the Union government should set up small offices of pollution control board and...
Doctors

Preventive Health Care is key to long life: Experts

Preventive Health Care is key to long life: Experts New Delhi: The medical community from India, Asia Pacific and...
Medicine

Antibiotics to group into categories to combat misuse: Experts

In a bid to combat the problem of overuse and underuse of antibiotics in India, experts are mulling if antibiotics can be grouped into...
FDA Regulators DCO

Mashelkar Committee

The Government of India constituted an Expert Committee under the chairmanship of Dr. R.A. Mashelkar to examine...
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...
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...
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....
DCGI CDSCO

DCGI gives permission to conduct Phase III trial for two-dose C-19 vaccine

India’s drug regulator Drugs Controller General of India (DCGI) has given permission to Zydus Cadila for conducting Phase III trial on the two-dose regimen...
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,...
DCGI CDSCO

Sputnik Single Dose Vaccine gets DCGI nod for Phase-III trials in India

NEW DELHI: The Drugs Controller General of India (DCGI) has granted permission for the conducting of the Phase III bridging trials of Sputnik Light on the...
DCGI CDSCO

DCGI asks State FDAs to restrict Tolperisone FDC for these usage only

Download DCGI's letter dated 01-09-2021 The Drugs Controller General (India) has asked the State drug controllers to restrict the...

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