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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

    Biocon unveils Liraglutide for diabetes, obesity in Netherlands

    Biocon unveils Liraglutide for diabetes, obesity in Netherlands

    Ruchika Sharma15 Dec 2025 12:14 PM IST
    Bengaluru: Biocon Limited, a global biopharmaceutical company, has announced the launch of its GLP-1 peptide, Liraglutide, for diabetes (gVictoza) and...
    Judicious use of AI can be boon for healthcare pharma sectors: Dr Jitendra Singh

    Judicious use of AI can be boon for healthcare pharma sectors: Dr Jitendra Singh

    Ruchika Sharma15 Dec 2025 11:15 AM IST
    New Delhi: Union Minister of State (Independent Charge) for Science & Technology Dr Jitendra Singh has emphasized that judicious use of...
    Biocon to make Biocon Biologics a wholly owned arm

    Biocon Biologics signs settlement, license agreement to commercialize biosimilar Aflibercept worldwide

    Ruchika Sharma14 Dec 2025 4:30 PM IST
    Bengaluru: Biocon Biologics Ltd, a fully integrated global biosimilars company and subsidiary of Biocon Ltd, has announced a new settlement...
    JnJ bags USFDA nod for Akeega plus prednisone for prostate cancer

    JnJ bags USFDA nod for Akeega plus prednisone for BRCA2 mutated metastatic castration sensitive prostate cancer

    Ruchika Sharma14 Dec 2025 3:00 PM IST
    Horsham: Johnson & Johnson has announced the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Application...
    Bayer-Regeneron Aflibercept 8 mg recommended for EU approval for third retinal indication

    Bayer-Regeneron Aflibercept 8 mg recommended for EU approval for third retinal indication

    Ruchika Sharma14 Dec 2025 2:00 PM IST
    Berlin: Bayer has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended...
    Merck Receives Positive EU CHMP Opinion for Expanded Use of Winrevair in Adults with Pulmonary Arterial Hypertension

    Merck receives positive EU CHMP opinion for expanded use of Winrevair in adults with Pulmonary Arterial Hypertension

    Ruchika Sharma14 Dec 2025 12:45 PM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the European Medicines Agency’s Committee for Medicinal...
    Sanofi gets approval for 2 rare hematologic diseases medicines in China

    Sanofi gets approval for 2 rare hematologic diseases medicines in China

    Ruchika Sharma14 Dec 2025 11:30 AM IST
    These two approvals expand Sanofi's rare hematology portfolio in China.
    GSK Nucala receives positive EMA Committee opinion for COPD

    GSK Nucala receives positive EMA Committee opinion for COPD

    Ruchika Sharma13 Dec 2025 3:32 PM IST
    London: GSK has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended the...
    Aurobindo Pharma arm API facility gets 3 observations from USFDA

    Aurobindo Pharma arm API facility receives 3 observations from USFDA

    Ruchika Sharma13 Dec 2025 12:58 PM IST
    Hyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (USFDA) concluded the inspection with three...
    Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

    Dr Reddy's Labs gets 5 USFDA observations for Srikakulam facility

    Ruchika Sharma13 Dec 2025 12:17 PM IST
    Hyderabad: Dr Reddy's Labs has announced that the United States Food & Drug Administration (USFDA) has completed a GMP and a...
    GSK Blujepa gets USFDA approval as oral option for uncomplicated urogenital gonorrhoea

    GSK Blujepa gets USFDA approval as oral option for uncomplicated urogenital gonorrhoea

    Ruchika Sharma13 Dec 2025 11:30 AM IST
    London: GSK has announced that the US Food and Drug Administration (FDA) has approved a supplemental New Drug Application for gepotidacin as an...
    Lupin gets seven USFDA observations for Goa facility

    Granules Life Sciences facility receives EIR from USFDA

    Ruchika Sharma13 Dec 2025 10:30 AM IST
    Hyderabad: Granules India has announced that Granules Life Sciences Private Limited, a wholly owned subsidiary of the company situated in...
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