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
DCGI asks state DCs to provide data on Oxytocin to curb its illegal movement in India - PharmaBiz, 1 month ago
Commerce Ministry to meet DCGI, Pharmexcil to discuss exporters issue soon - PharmaBiz, 2 months ago
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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 ...PharmaBiz, 1 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 ...PharmaBiz, 1 month ago DCGI to approve clinical trial proposals for new drugs approved abroad, FDCs, subsequent new drugs & vaccines PharmaBiz, 1 month ago
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 ...PharmaBiz, 1 month ago CDSCO forms 5-member panel headed by Dr. Jagashetty to review manpower structure of CDL, Kolkata PharmaBiz, 1 month ago
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 ...PharmaBiz, 1 month ago
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.com, 2 hours ago
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 ...PharmaBiz, 14 hours ago Ranbaxy Laboratories : Labs to take its novel drug Synriam to Africa 4 Traders, 2 days ago Ranbaxy Gets the Nod to Commence Distribution of Its Anti-malarial Drug in 7 African Countries MedIndia, 3 days ago Ranbaxy gets nod to sell drug treating malaria in 7 African nations DNA India, 3 days ago
Posted by admin on · Leave a Comment Athanasia Zagorianou Strathclyde University, Master in Human Rights Law, Researcher & Member, Trustees Council, Citizens Rights Watch (CRW) E-mail: firstname.lastname@example.org , / email@example.com ...Global Education Magazine, 1 day ago
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 India, 4 days ago Clinical Trials in India: 370 Killed Since Feb 2013, Only 21 Paid Compensation International Business Times India, 4 days ago India computes new formula to compensate clinical trial deaths Economic Times, 4 days ago 370 die in clinical trials in 2 years, kin of only 21 get compensation Times of India, 4 days ago
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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 India, 4 days ago
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