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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

    EMA Committee recommends marketing nod for Bayer advanced prostate cancer drug darolutamide

    EMA Committee recommends marketing nod for Bayer advanced prostate cancer drug darolutamide

    Ruchika Sharma22 Jun 2025 1:00 PM IST
    Berlin: Bayer has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has...
    CDSCO Panel Approves GSKs Proposal to Double Indian Patient Pool in Dostarlimab Trial

    GSK application for expanded use of RSV vaccine in adults aged 18-49 accepted in Japan

    Ruchika Sharma22 Jun 2025 11:30 AM IST
    GSK plc has announced that Japan's Ministry of Health, Labour and Welfare (MHLW) has accepted the company's regulatory application to expand the use...
    JnJ receives USFDA Approval for updated Varipulse Platform Irrigation Rate

    Johnson & Johnson MedTech unveils VOLT Wrist, Proximal Humerus Plating Systems in US

    Ruchika Sharma22 Jun 2025 10:15 AM IST
    These address a critical gap in treating two common fractures.
    Eli Lilly reports strong response for Mounjaro in India

    Eli Lilly reports strong response for Mounjaro in India amid rising diabetes, obesity rates

    Ruchika Sharma21 Jun 2025 4:30 PM IST
    Bengaluru: U.S. pharmaceutical giant Eli Lilly has reported a "positive" response to its blockbuster drug Mounjaro in India, as the company...
    Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

    Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

    Ruchika Sharma21 Jun 2025 3:56 PM IST
    Beerse: Janssen-Cilag International NV, a Johnson & Johnson company, has announced that the Committee for Medicinal Products for Human Use...
    India offers Rs 10 crore reward for new drug to treat sickle cell disease

    India offers Rs 10 crore reward for new drug to treat sickle cell disease

    Ruchika Sharma21 Jun 2025 12:32 PM IST
    New Delhi: The government has announced a prize of Rs 10 crore to develop a drug for the treatment of sickle cell disease.There is only a single drug...
    Biocon appoints Ekta Agarwal as Interim Company Secretary, Compliance Officer

    Biocon concludes Rs 4500 crore equity fundraise through QIP

    Ruchika Sharma21 Jun 2025 11:30 AM IST
    Bengaluru: Biocon Limited, a global biopharmaceutical company, has announced the successful completion of a Qualified Institutions...
    Granules India Hyderabad API facility gets 1 USFDA observation

    Granules India Bonthapally API facility gets 1 USFDA observation

    Ruchika Sharma20 Jun 2025 6:14 PM IST
    Hyderabad: Granules India has announced that the Company's Bonthapally API Unit-I facility has concluded a U.S. Food and Drugs...
    Counterfeit version of Sun Pharma Cholesterol lowering drugs worth Rs 3 lakhs seized in Hyderabad

    Counterfeit version of Sun Pharma Cholesterol lowering drugs worth Rs 3 lakhs seized in Hyderabad

    Ruchika Sharma20 Jun 2025 3:57 PM IST
    Telangana: Drugs Control Administration, Telangana, has seized counterfeit versions of cholesterol-lowering drugs, 'Rosuvas F 20' and...
    Vinay Prasad named Chief Medical, Science Officer of USFDA: Report

    Vinay Prasad named Chief Medical and Science Officer at USFDA: Report

    Ruchika Sharma20 Jun 2025 3:03 PM IST
    Bengaluru: The U.S. Food and Drug Administration (USFDA) top vaccine official, Vinay Prasad, has been appointed as the agency's new chief medical...
    Sanofi Dupixent

    Sanofi Dupixent gets USFDA nod for bullous pemphigoid treatment in adults

    Ruchika Sharma20 Jun 2025 12:15 PM IST
    Paris: Sanofi has received approval from the US Food and Drug Administration (FDA) for Dupixent (dupilumab) for the treatment of adult patients...
    Natco Pharma gets 7 USFDA observations for Kothur Pharma Division

    USFDA inspection: Natco Pharma gets 7 observations for Kothur Pharma Division

    Ruchika Sharma20 Jun 2025 11:31 AM IST
    Hyderabad: Natco Pharma Limited has announced that the U.S. Food and Drug Administration (FDA) has concluded an inspection with seven...
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