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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 [email protected] Contact no. 011-43720751

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    • Ruchika Sharma

    Articles By : Ruchika Sharma

    Emcure Pharma Gets CDSCO Panel Nod to Conduct Phase IV Trial on Drospirenone Tablets

    USFDA issues EIR for Emcure Pharma Pune API facility

    Written By Ruchika Sharma19 April 2025 12:15 PM IST
    Pune: In a recent BSE filing, Emcure Pharma has informed that the Company has received the Establishment Inspection Report (EIR) from the...
    hypertension

    JB Chemicals gets USFDA nod for hypertension drug Bisoprolol

    Written By Ruchika Sharma19 April 2025 11:21 AM IST
    Mumbai: J.B. Chemicals & Pharmaceuticals Limited has announced that the company has received approval from the United States Food and...
    Boehringer Ingelheim appoints Shashank Deshpande as Chairman of Board of Managing Directors

    Boehringer Ingelheim appoints Shashank Deshpande as Chairman of Board of Managing Directors

    Written By Ruchika Sharma18 April 2025 4:31 PM IST
    Ingelheim: Boehringer Ingelheim has announced that Shashank Deshpande, member of the Board of Managing Directors, has been appointed Chairman of the...
    USFDA Approves Corcept Therapeutics Ovarian Cancer Drug Lifyorli

    USFDA approves Alembic Pharma anticonvulsant drug Carbamazepine

    Written By Ruchika Sharma18 April 2025 12:47 PM IST
    Vadodara: Alembic Pharmaceuticals Limited announced that the US Food & Drug Administration (USFDA) has approved its Abbreviated New Drug...
    USFDA updates Camzyos label to reduce echocardiography monitoring requirements, contraindications: Bristol Myers Squibb

    USFDA updates Camzyos label to reduce echocardiography monitoring requirements, contraindications: Bristol Myers Squibb

    Written By Ruchika Sharma18 April 2025 11:00 AM IST
    Princeton: Bristol Myers Squibb has announced that the U.S. Food and Drug Administration (FDA) has updated the U.S. Prescribing Information for...
    Lupin Gets USFDA Approval for Xigduo XR Generic Dapagliflozin-Metformin Tablets

    USFDA issues EIR for Lupin Nagpur Injectable facility

    Written By Ruchika Sharma17 April 2025 3:00 PM IST
    Mumbai: Global pharma major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States Food...
    Abbott India appoints Anushree Kunhambu as Associate Director - New Product Introduction and Therapy Area Strategy

    Abbott India names Anushree Kunhambu as Associate Director - New Product Introduction and Therapy Area Strategy

    Written By Ruchika Sharma16 April 2025 3:35 PM IST
    Mumbai: Abbott India has announced the appointment of Anushree Kunhambu as Associate Director - New Product Introduction and Therapy Area...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    Laurus Labs gets USFDA EIR for Atchutapuram facility

    Written By Ruchika Sharma16 April 2025 11:30 AM IST
    Andhra Pradesh: Laurus Labs has announced that the company has received the Establishment Inspection Report (EIR) from the United States Food...
    Shilpa Biologicals, Stein Cares Ink Exclusive Biosimilar Licensing Pact for Latin America

    Boehringer Ingelheim, Cue Biopharma partner to develop next generation treatment for autoimmune, inflammatory diseases

    Written By Ruchika Sharma16 April 2025 10:30 AM IST
    Boston: Boehringer Ingelheim and Cue Biopharma, Inc. have announced a strategic research collaboration and license agreement to develop and...
    Bristol Myers Squibb Wins USFDA Approval for Opdivo Combo in Hodgkin Lymphoma

    Bristol Myers Squibb heart disease drug fails to meet main goals in late-stage study

    Written By Ruchika Sharma16 April 2025 9:30 AM IST
    Princeton: Bristol Myers Squibb has announced the Phase 3 ODYSSEY-HCM trial evaluating Camzyos (mavacamten) for the treatment of adult...
    Biocon Biologics Secures BB+ Rating Upgrade from S&P on Improved Financial Metrics

    Biocon Biologics secures market entry date for ophthalmology drug Yesafili in US

    Written By Ruchika Sharma15 April 2025 4:18 PM IST
    Additionally, Biocon Biologics secured a settlement agreement in Canada with Bayer and Regeneron Pharma for launch of YESAFILI no later than July 1,...
    AstraZeneca Pharma India surrenders marketing authorisation for specific indication of Olaparib

    AstraZeneca Pharma India surrenders marketing authorisation for specific indication of Olaparib

    Written By Ruchika Sharma15 April 2025 3:46 PM IST
    Bangalore: AstraZeneca Pharma India Limited has surrendered its marketing authorisation for Olaparib film-coated tablets 100mg and 150mg...
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