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About 143 results for "dcgi"

DCGI asks Chaitanya Hospital to stop treatments with stem cell...

The Drug Controller General of India (DCGI) has asked the Pune-based Chaitanya Hospital to stop the treatments with stem cell products to the patients in the name of clinical trial with immediate effect. The DCGI's action comes in pursuance to the ... PharmaBiz, 2 days ago

2 images for "dcgi"

Slate Magazine, 3 weeks ago
Down to Earth, 2 months ago

Industry urges DCGI to treat all SLA-approved FDC drugs prior to 2008 as rational

Even as the contentious FDC issue still remains unresolved for quite some time with the DCGI insisting on CDSCO approval for all the FDCs, the pharmaceutical industry in the country has asked the DCGI to consider all the SLA-approved FDC drugs being ...
 PharmaBiz1 week ago

Apex Committee turns down DCGI's proposal on trial approval for FDCs, subsequent new drugs, vaccines

The Union health ministry's Apex Committee, headed by Union health secretary, has turned down a proposal by the Drugs Controller General of India (DCGI) to dispose of clinical trial proposals of new drugs already approved in other countries, fixed ...
 PharmaBiz1 month ago DCGI to approve clinical trial proposals for new drugs approved abroad, FDCs, subsequent new drugs & vaccines  PharmaBiz1 month ago

DCGI constitutes committee to simplify various Forms, Formats to minimum possible level

As part of the Central government governance reforms programme, the Central Drugs Standard Control Organisation (CDSCO) will soon simplify the various Forms and Formats to minimum possible level for the benefit of the stakeholders. According to ...
 PharmaBiz1 month ago CDSCO forms 5-member panel headed by Dr. Jagashetty to review manpower structure of CDL, Kolkata  PharmaBiz1 month ago

DCGI to provide WC certificate to exporters on submission of 6-month stability data

The Central Drugs Standard Control Organisation (CDSCO) will soon start issuing the mandatory Written Confirmation (WC) certificate to the Indian API exporters to European Union (EU) on providing the 6 months long term stability data against the ...
 PharmaBiz1 month ago

Probing manufacture of generic drugs without testing: Nadda

The government is investigating reports of generic versions of some medicines being manufactured without proper testing, Health Minister J.P. Nadda Friday told parliament. In a written reply in the Lok Sabha, Nadda said that the government was ...
 ProKerala.com2 hours ago
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MedIndia

Novartis gets clinical trial waiver for its Cushing's disease drug Pasireotide

The Union health ministry has given permission to multinational drug company Novartis to import and market its Cushing's disease drug, Pasireotide, without conducting any local clinical trial on Indian population. Senior officials said that the ...
 PharmaBiz14 hours ago Ranbaxy Laboratories : Labs to take its novel drug Synriam to Africa  4 Traders2 days ago Ranbaxy Gets the Nod to Commence Distribution of Its Anti-malarial Drug in 7 African Countries  MedIndia3 days ago Ranbaxy gets nod to sell drug treating malaria in 7 African nations  DNA India3 days ago
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Monitoring the Greek Case during the Financial Crisis

Posted by admin on ยท Leave a Comment Athanasia Zagorianou Strathclyde University, Master in Human Rights Law, Researcher & Member, Trustees Council, Citizens Rights Watch (CRW) E-mail: nassia_izago@yahoo.gr , / zagorianoua@gmail.com ...
 Global Education Magazine1 day ago
International Business Times India

370 clinical trial deaths, just 21 compensations in 2 years

A total of 370 persons have reportedly died during clinical trials in India since February 2013, but compensation have been paid in only 21 cases, according to government data. According to a senior official from the Union Health Ministry, these ...
 Business Standard India4 days ago Clinical Trials in India: 370 Killed Since Feb 2013, Only 21 Paid Compensation  International Business Times India4 days ago India computes new formula to compensate clinical trial deaths  Economic Times4 days ago 370 die in clinical trials in 2 years, kin of only 21 get compensation  Times of India4 days ago
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Surprises can be unpleasant

The US FDA (Food & Drug Administration) has made a virtue of surprising Indian generic companies with unannounced inspections of various plants across the country. Such visits have become too frequent, with the American drug regulator catching ...
 Business Standard India4 days ago
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