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Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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    Articles By : Ruchika Sharma

    Covishield protection diminishes after 3 months: Lancet study

    Covishield protection diminishes after 3 months: Lancet study

    Ruchika Sharma24 Dec 2021 9:30 AM IST
    London: The protection offered by the Oxford-Astra Zeneca COVID-19 vaccine declines after three months of receiving two doses of the preventive,...
    Serum Institute waives indemnity over AstraZeneca COVID vaccine for refugees

    Serum Institute waives indemnity over AstraZeneca COVID vaccine for refugees

    Ruchika Sharma24 Dec 2021 9:00 AM IST
    New Delhi: The Serum Institute of India (SII) has waived its protection from legal liabilities for any AstraZeneca-Oxford COVID-19 shots it supplies...
    Booster dose of AstraZeneca COVID vaccine effective against Omicron

    Booster dose of AstraZeneca COVID vaccine effective against Omicron

    Ruchika Sharma23 Dec 2021 3:52 PM IST
    UK: Citing the Oxford University lab study , drug major AstraZeneca has announced that the booster dose of the company's COVID vaccine Vaxzevria...
    Hamdard Labs enters OTX segment, launches 13 new products

    Hamdard Labs enters OTX segment, launches 13 new products

    Ruchika Sharma23 Dec 2021 2:23 PM IST
    New Delhi: Health and wellness firm Hamdard Laboratories on Monday said it has expanded its product portfolio with the introduction of 13 new products...
    Pfizer COVID drug Paxlovid gets USFDA emergency use nod

    Pfizer COVID drug Paxlovid gets USFDA emergency use nod

    Ruchika Sharma23 Dec 2021 12:54 PM IST
    New York: Pfizer Inc. has recently announced that the U.S. Food and Drug Administration (FDA) has authorized the emergency use of PAXLOVID...
    Serum Institute chief picks up 20 percent stake in Wakau

    Serum Institute chief picks up 20 percent stake in Wakau

    Ruchika Sharma23 Dec 2021 12:19 PM IST
    New Delhi: Serum Institute of India (SII) Chief Adar Poonawaalla has picked up a 20 per cent stake in Wakau Interactive, a short-video sharing...
    Zydus gets USFDA nod to Pimavanserin for Parkinsons disease-linked psychosis

    Zydus gets USFDA nod to Pimavanserin for Parkinson's disease-linked psychosis

    Ruchika Sharma23 Dec 2021 11:55 AM IST
    Ahmedabad: Drugmaker, Zydus Cadila has received tentative approval from the US Food and drug Administration (USFDA) to market Pimavanserin Tablets,...
    WHO advisory group issues interim recommendations for Covovax use

    WHO advisory group issues interim recommendations for Covovax use

    Ruchika Sharma23 Dec 2021 10:00 AM IST
    Gaithersburg: Novavax, Inc. has announced that the World Health Organization (WHO) Strategic Advisory Group of Experts on Immunization...
    Strides Pharma biotech division gets CDSCO nod to manufacture, export Sputnik Light

    Strides Pharma biotech division gets CDSCO nod to manufacture, export Sputnik Light

    Ruchika Sharma22 Dec 2021 1:22 PM IST
    Bengaluru: Stelis Biopharma Limited, the biotech division of Strides Pharma Science Limited, has commissioned its large-scale fully integrated...
    MSN Pharma concludes USFDA audit with zero observations

    MSN Pharma concludes USFDA audit with zero observations

    Ruchika Sharma22 Dec 2021 12:09 PM IST
    Hyderabad: MSN Pharmaceuticals Inc. (MSNPI), a wholly-owned subsidiary of MSN Group of Companies, based out of Piscataway, New Jersey, USA has...
    Takeda receives USFDA Complete Response Letter for Budesonide Oral Suspension

    Takeda receives USFDA Complete Response Letter for Budesonide Oral Suspension

    Ruchika Sharma22 Dec 2021 11:30 AM IST
    Osaka: Takeda Pharmaceutical Company Limited has announced that it has received a Complete Response Letter (CRL) from the U.S. Food and Drug...
    Covid-19: Sputnik V due to submit vaccine data to WHO by December end

    Covid-19: Sputnik V due to submit vaccine data to WHO by December end

    Ruchika Sharma22 Dec 2021 11:00 AM IST
    Geneva: The Russian maker of the COVID-19 Sputnik V vaccine is due to submit its latest clinical data by the end of December, with manufacturing site...
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