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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

    Entresto Patent Expiry to Weigh on Novartis as Profit Seen Falling in 2026

    Novartis Cosentyx gets USFDA approval

    Ruchika Sharma26 Dec 2021 9:45 AM IST
    Basel: Novartis has announced the US Food and Drug Administration (USFDA) has approved Cosentyx (secukinumab) for the treatment of active...
    Biogen gets USFDA Fast Track designation for lecanemab

    Biogen gets USFDA Fast Track designation for lecanemab

    Ruchika Sharma26 Dec 2021 9:30 AM IST
    Tokyo: Eisai Co., Ltd. and Biogen Inc. have announced that lecanemab, an investigational anti-amyloid beta (Aβ) protofibril antibody for the...
    CanSino Biologics COVID vaccine shows 57.5 percent efficacy in Phase 3 study

    CanSino Biologics COVID vaccine shows 57.5 percent efficacy in Phase 3 study

    Ruchika Sharma26 Dec 2021 9:15 AM IST
    Beijing: CanSino Biologics Inc's vaccine was 57.5% effective against symptomatic COVID-19 and 91.7% against severe disease four weeks or longer after...
    Misquoted: Experts clarify on Lancet study claiming protection offered by Covishield declines after 3 months

    Misquoted: Experts clarify on Lancet study claiming protection offered by Covishield declines after 3 months

    Ruchika Sharma25 Dec 2021 3:40 PM IST
    New Delhi: The Lancet study, which reportedly states that the protection offered by the Oxford AstraZeneca Covid-19 vaccine Covishield declines after...
    Merck, Ridgeback Molnupiravir gets special approval for emergency in Japan

    Merck, Ridgeback Molnupiravir gets special approval for emergency in Japan

    Ruchika Sharma25 Dec 2021 2:46 PM IST
    Kenilworth: Merck, known as MSD outside the United States and Canada, and Ridgeback Biotherapeutics have announced that Japan's Ministry of Health,...
    DCGI seeks Serum Institute to submit more data for Covovax emergency authorization

    DCGI seeks Serum Institute to submit more data for Covovax emergency authorization

    Ruchika Sharma25 Dec 2021 2:18 PM IST
    New Delhi: The Drugs Controller General of India (DCGI) has raised queries and sought more data from Serum Institute of India over its application...
    Lupin bags USFDA nod for generic equivalent of Edarbi Tablets

    Lupin bags USFDA nod for generic equivalent of Edarbi Tablets

    Ruchika Sharma25 Dec 2021 2:16 PM IST
    Mumbai: Global pharma major Lupin Limited has announced that the company has received tentative approval from the United States Food and Drug...
    Roche at-home COVID rapid test gets USFDA approval

    Roche at-home COVID rapid test gets USFDA approval

    Ruchika Sharma25 Dec 2021 1:01 PM IST
    Basel: Roche has recently announced that the U.S. Food and Drug Administration (USFDA) has granted Emergency Use Authorization (EUA) for its...
    Sucharita Rao Palepu appointed as Granules India independent director

    Sucharita Rao Palepu appointed as Granules India independent director

    Ruchika Sharma24 Dec 2021 1:22 PM IST
    New Delhi: Drug maker, Granules india has recently announced the appointment of Mrs. Sucharita Rao Palepu as an Additional Director, categorized as...
    Biocon arm gets DCGI nod to initiate clinical study for Itolizumab

    Biocon arm gets DCGI nod to initiate clinical study for Itolizumab

    Ruchika Sharma24 Dec 2021 1:13 PM IST
    Itolizumab is a clinical-stage, first-in-class anti-CD6 monoclonal antibody that selectively targets the CD6-ALCAM pathway.
    Finally Molnupiravir gets USFDA nod

    Finally Molnupiravir gets USFDA nod

    Ruchika Sharma24 Dec 2021 11:36 AM IST
    Kenilworth: A day after Pfizer's Paxlovid bagged the U.S. Food and Drug Administration (USFDA) Emergency Use Authorization (EUA) nod, Merck's...
    Pharma will give momentum in 2022, says OPPI

    Pharma will give momentum in 2022, says OPPI

    Ruchika Sharma24 Dec 2021 11:15 AM IST
    New Delhi: Having contributed to the world during the challenging pandemic times by supplying 60 per cent of the global COVID-19 vaccine requirements,...
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