-Live Mint With a new political transition, it may be a good idea for the new government to work on an idea as to how to enable all health workers across the country to have data-enabled smartphones If you have no electricity, you can survive despite inconvenience; if you have no pucca house, you still survive on thatched shelters; if you have bad roads, you can still communicate on the patched...
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Conflict of interest in setting norms for pharmaceuticals in WHO -Rema Nagarajan
-The Times of India NEW DELHI: The World Health Organisation's (WHO) work of setting up norms and standards for production of medicines seems to be flawed by a fundamental conflict of interest. At the heart of its standard setting work is an entity the International Conference on Harmonization (ICH) in which majority of the WHO member countries have no voting rights and which is dominated by pharmaceutical industry groups. This glaring...
More »Many Indians Feel Custodial Torture Justified: Amnesty
-Outlook Fear of torture in custody is widely prevalent among people across the world though respondents in many countries, including India, felt that the practice can sometimes be justified, a survey by Amnesty International (AI) has found. A new global survey by the human rights watchdog covering more than 21,000 people in 21 countries reveals that the fear of custodial torture spans all continents, AI said in a release today. According to AI,...
More »Fixing India’s healthcare system-AK Shiva Kumar
-Live Mint Strong political commitment is needed to build a system of universal health coverage and better regulations Life expectancy in India has more than doubled since independence, to 65 years, from just 32 in 1950. The infant mortality rate has been cut by two-thirds since 1971. Smallpox and guinea worm have been eradicated, the spread of HIV/AIDS has been contained, and the World Health Organization has declared India polio-free. Yet for all...
More »Onus on the state-Sagnik Dutta
-Frontline A Delhi High Court verdict says the State government is bound to ensure that poor and vulnerable sections of society have access to treatment for rare and chronic diseases. SEVEN-YEAR-OLD Mohammed Ahmed Khan looked on helplessly as his father, Sirajuddin, narrated the sordid tale of the loss of four of his children to Gaucher's disease, a rare genetic disease that requires lifelong, exorbitantly expensive enzyme replacement therapy. Sirajuddin, a rickshaw...
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