Govt failed to get FAC okay for Yettinahole project: Petitioner

Agencies
August 22, 2017

New Delhi, Aug 22: A petitioner opposing the Yettinahole drinking water project near Sakleshpur informed the National Green Tribunal on Monday that the Karnataka government failed to obtain mandatory Forest Advisory Committee (FAC) approval since it was an irrigation project and required large scale diversion of forest land.

Advocate Ritwick Dutta representing petitioner K N Somashekhar said before the NGT bench headed by Justice Javed Rahim that though the state government claimed that it is a drinking water project, in reality it is a minor irrigation project where water will be drawn from the Western Ghats and diverted to fill the lakes in Kolar and Chikkaballapur districts.

Besides, the project required the approval of the FAC and not the Regional Forest Experts committee as claimed by the state government, he said.

Alleging that the entire project report prepared by the state government was flawed, the advocate said the Sakleshpur region of the Western Ghats did not have sufficient water as projected by the state government.

The advocate also said that according to the Kasturirangan report, no major irrigation project should come up in the ecologically sensitive Western Ghats. If the current project comes up in region, it would be a big threat to the ecology of the Western Ghats, he said.

The bench allowed the Karnataka government to make its arguments on September 12 and 13.

Comments

Kumar
 - 
Tuesday, 22 Aug 2017

Should abandon that project

Vinod
 - 
Tuesday, 22 Aug 2017

Another thuglak project.. it wont be practical. if made practical also, people wont get its benefit

Hari
 - 
Tuesday, 22 Aug 2017

People dont want yettinahole.. in public both bjp and cong opposed the project.. still why sticking on that project.

Ganesh
 - 
Tuesday, 22 Aug 2017

Why still yetinahole...!

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News Network
May 13,2020

Shivamogga, May 12: As many as six medical staff members, attached to the Shivamogga district hospital, who were members of the Corona Warriors team, were suspended for raising concerns over inadequate facilities, available to the frontline workers.

According to official sources, among the six, who were suspended by the Hospital Director, included three staff nurses and other supporting staff in the hospital.

The cause for the retaliation with punishment, was following concerns raised by the medical staff over aweful facilities, made available to them by the Hospital authorities.

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News Network
July 16,2020

Byndoor, Jul 16: Byndoor Police Station in Kundapur taluk of Udupi District, has been sealed for the second time in a month, after three personnel including an ASI were tested positive for Covid-19 on Thursday.

All the three including a lady Home Guard have been admitted to the designated Covid Hospital.

Last month the Station was sealed after staff had tested positive.

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coastaldigest.com web desk
July 1,2020

The United States of America has bought almost the entire world's supply of remdesivir, one of just two drugs proven to treat COVID-19. 

“President Trump has struck an amazing deal to ensure Americans have access to the first authorised therapeutic for Covid-19,” said the US health and human services secretary, Alex Azar. 

“To the extent possible, we want to ensure that any American patient who needs remdesivir can get it. The Trump administration is doing everything in our power to learn more about life-saving therapeutics for Covid-19 and secure access to these options for the American people.”

The announcement implies that no other country in the world will be able to buy remdesivir for next three months at least.

The anti-viral drug patented by the US-based Gilead biotech firm is the only one approved by the European Medicines Agency (EMA) to treat patients with the novel coronavirus.

The Trump administration has already shown that it is prepared to outbid and outmanoeuvre all other countries to secure the medical supplies it needs for the US.

“They’ve got access to most of the drug supply [of remdesivir], so there’s nothing for Europe,” said Dr Andrew Hill, senior visiting research fellow at Liverpool University.

Remdesivir, the first drug approved by licensing authorities in the US to treat Covid-19, is made by Gilead and has been shown to help people recover faster from the disease. 

The first 140,000 doses, supplied to drug trials around the world, have been used up. The Trump administration has now bought more than 500,000 doses, which is all of Gilead’s production for July and 90% of August and September.

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