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COVID-19 spreading at fast pace, next 4 weeks critical: Centre

”The intensity of the pandemic has increased and it is spreading faster than last time. In some states, it (the condition) is worse than others but the upswing (in cases) can be observed across the country,” he said.

”People’s participation is vital to control the second wave. The next four weeks are going to very critical. The entire country has to come together and make efforts to fight the pandemic.”

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Harsh Vardhan launches Integrated Health Information Platform

“In addition to tracking 33 diseases now as compared to the earlier 18 diseases, it shall ensure near-real-time data in digital mode, having done away with the paper-mode of working,” the health minister said.

Terming this as the world’s biggest online disease surveillance platform, he stated that it is in sync with the National Digital Health Mission and fully compatible with the other digital information systems presently being used in India. The refined IHIP with automated -data will help in a big way in real-time data collection, aggregation & further analysis of data that will aid and enable evidence-based policymaking, Vardhan explained.

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IRDAI tightens product and pricing regulations to check undercutting or inflating of premiums by general insurers

Analysts point out that, such regulations to check undercutting of premiums, that have been happening since detariffing was launched in the Indian general insurance industry in 2007 were overdue. Such cut throat unethical competition was generating huge underwriting losses in the domestic general insurance indstry which was not good for the financial viabilities of the players who are saddled with underwriting losses and even net losses even after so many years of operations..     

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Health Minister Vardhan approves National Policy for Rare Diseases, 2021

“The Rare Diseases Policy aims to lower the high cost of treatment for rare diseases with increased focus on indigenous research with the help of a national consortium to be set up with the Department of Health Research, Ministry of Health and Family Welfare as convenor,” it said.

The policy also talks about the creation of national hospital based registry of rare diseases so that adequate data is available for definition of such diseases and for research and development related to rare diseases within the country, it said.

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