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CBI, I-T on Ramdev trail by Saroj Nagi

-The Hindustan Times   After the midnight purge, Baba Ramdev now faces CBI and income tax department scrutiny. The government activated the two agencies to look into the companies, properties and audit accounts of the yoga guru and his aides on Sunday, the day it broke up his fast, evicting him and his supporters from the Ramlila Maidan. Initial paperwork has begun. Under the scanner is the functioning of about 200 companies with...

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Clinical trials claimed 25 lives in 2010, only 5 paid compensation by Kounteya Sinha

Rs 3 lakh – that's the price a pharmaceutical company has paid to the family of a person who died in their clinical trial. Others weren't even this lucky. According to the Drug Controller General of India's (DCGI) records, 25 people died in clinical trials carried out by nine pharmaceutical companies in 2010. Families of five of these victims received "compensation for trial related death" — the amount ranging from Rs...

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Raxaul'skala-paanisets stage for showdown by Shoumojit Banerjee

Pantoka is a beehive of activity. The spirit of protest in this small hamlet on the India-Nepal border is not a simple case of topical environmental awakening; it is a desperate struggle for life in which more than 1 lakh lives are at stake. Today, the first day of June, the citizens of Bihar's Raxaul sub-division in East Champaran district will stage a massive blockade on National Highway 28A, shutting off...

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Violations May Hit Vaccination Plans by Ranjit Devraj

After a government report confirmed major ethical violations in trials of Human Papilloma Virus (HPV) vaccines on Indian schoolgirls, senior doctors are calling for transparency in clinical trials conducted under private-public partnerships. The report is yet to be placed in the public domain, but its contents were revealed early May by senior doctors who assisted in its preparation, sparking outrage among public health advocates and women’s rights groups. HPV is an umbrella...

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Details of patented drugs to be made public by CH Unnikrishnan

To increase transparency, India’s patent regulator will soon make public details about patented drugs which include whether domestic demand for these medicines is met at a reasonable price. Patent holders in the country are required to submit once every year the so-called working details which include the quantity and value of a product that is sold, manufacturing base, quantity of production or imports, and a statement on whether public requirement has...

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