Only Marginal Difference In Purchase Price Of Covishield, Covaxin For Centre: MoS Health

New Delhi : The Centre is purchasing Covishield and Covaxin doses at the rate of Rs 205 and Rs 215 per dose, respectively, and there is only a marginal difference in the purchase price of the two vaccines for the government, the Lok Sabha was informed on Friday. In a written reply to Unstarred Question No. 912, Minister of State for Health Bharati Pravin Pawar also said that the government is not facing any difficulty in procuring and arranging vaccines for states and Union territories (UTs).

In fact, the Government of India has been supplying vaccines free of cost to the states/UTs for administration to prioritised beneficiaries as recommended by the National Expert Group on Vaccine Administration for COVID-19 (NEGVAC).

“Advance visibility of these allocations, that is, the total doses of vaccine that would be available to a state and UT, is provided to them 15 days in advance, so as to enable them to plan for acceleration of vaccination coverage while being cognizant of the available vaccines,” the minister said.

The Government of India allocates vaccines to states/UTs based on criteria such as pro rata target population, progress of vaccination in the state and UT and vaccine wastage.

“According to the latest supply order, the Government of India is purchasing Covishield (exclusive of taxes) at the rate of Rs 205 per dose and Covaxin at the rate of Rs 215 per dose. There is only a marginal difference in the purchase price of the two vaccines for the Government of India,” Pawar said in the written reply.

As on July 20, 2021, a total of 42.52 crore doses of Covishield and Covaxin have been supplied for COVID-19 vaccination drive in India.

Till July, around Rs 8,071.09 crore has been spent on purchase of COVID-19 vaccines. The price of vaccine for procurement by the Government of India is negotiated by NEGVAC and its subgroups involving detailed deliberations with the vaccine manufacturers, the minister told the House in response to a separate Unstarred Question 786.

She further elaborated on the initiatives taken by the Union government to help Indian vaccine manufacturers who are in the process of developing COVID-19 vaccine which are in advance stage of trial.

The Department of Biotechnology (DBT) under the Ministry of Science and Technology is implementing ‘COVID Suraksha- the Indian COVID-19 Vaccine Development Mission’.

  • Related Posts

    WHO launches new primary health care course to strengthen health systems globally

    Health is a human right – yet not everyone can access the health services they need, when and where they need them, without financial hardship. Primary health care (PHC) provides…

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Bengaluru: The Central Council for Research in Ayurvedic Sciences (CCRAS) has called for stronger scientific evidence, safety monitoring and translation of research into market-ready technologies to improve the credibility and…

    Leave a Reply

    Your email address will not be published. Required fields are marked *

    You Missed

    Excellence of Accredited Hospitals to be judged on how Friendly they are with Patients

    Excellence of Accredited Hospitals to be judged on how Friendly they are with Patients

    WHO launches new primary health care course to strengthen health systems globally

    WHO launches new primary health care course to strengthen health systems globally

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A