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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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    • Ruchika Sharma

    Articles By : Ruchika Sharma

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

    Bristol Myers Squibb gets Positive EMA Committee opinion for subcutaneous formulation of Opdivo across Multiple Solid Tumor Indications

    Ruchika Sharma29 March 2025 5:47 PM IST
    Princeton: Bristol Myers Squibb has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency...
    AstraZeneca Gets SEC Nod to Update Lokelma Prescribing Information for Hyperkalemia Treatment

    AstraZeneca Pharma India to discontinue manufacturing, marketing of angina drug from April 1

    Ruchika Sharma29 March 2025 2:21 PM IST
    Bangalore: AstraZeneca Pharma India Limited has announced that the Company will be discontinuing the manufacturing and marketing of the product...
    Novartis concludes acquisition of Tourmaline Bio

    Novartis radioligand therapy Pluvicto gets USFDA nod for expanded indication

    Ruchika Sharma29 March 2025 1:15 PM IST
    Basel: Novartis has announced that the US Food and Drug Administration (FDA) has approved Pluvicto (lutetium Lu 177 vipivotide tetraxetan) for...
    Lupin three senior executives to retire

    Lupin three senior executives to retire in 2 days

    Ruchika Sharma29 March 2025 12:15 PM IST
    Mumbai: Global pharmaceutical giant Lupin has announced the retirement of its three senior executives.Naresh Gupta, President – API Plus &...
    Corcept Therapeutics

    USFDA approves Sanofi Qfitlia for hemophilia A or B with or without inhibitors

    Ruchika Sharma29 March 2025 11:30 AM IST
    Paris: Sanofi has announced that the Company has received approval from the US Food and Drug Administration (FDA) for Qfitlia...
    GSK arm Tesaro initiates litigation against AnaptysBio

    BioNTech vs CureVac: European Patent Office declares CureVac mRNA patent valid

    Ruchika Sharma28 March 2025 5:11 PM IST
    In a legal battle between BioNTech and CureVac, the European Patent Office declared a patent owned by CureVac valid.U.S.-listed shares of...
    DMER Releases Pharmacist, Lab Technician CBT Results 2025

    Procure medicines from Jan Aushadhi Kendras: Delhi Govt mandates its hospitals

    Ruchika Sharma28 March 2025 4:00 PM IST
    New Delhi: In an effort to ensure affordable and quality medicines for patients, the Delhi government has mandated the procurement of medicines...
    CDSCO Panel Denies Trial Waiver for Atropine, Asks Sun Pharma to Conduct Phase III Study

    Sun Pharma investee firm Lyndra Therapeutics ceased operations

    Ruchika Sharma28 March 2025 2:58 PM IST
    Vadodara: Sun Pharmaceutical Industries Limited's investee company, Lyndra Therapeutics Inc., has ceased operations due to insufficient funding...
    Sharon Bio Medicine fraud case: ED issues provisional attachment order

    Sharon Bio Medicine fraud case: ED issues provisional attachment order

    Ruchika Sharma28 March 2025 2:00 PM IST
    As part of the ongoing probe in the case of bank fraud against M/s Sharon Bio Medicine Limited and others, Directorate of Enforcement (ED),...
    JnJ Medtech bags USFDA nod for TRUFILL n-BCA Liquid Embolic System for Symptomatic Chronic Subdural Hematoma

    Johnson & Johnson MedTech introduces Dualto Energy System for use across surgical treatment approaches

    Ruchika Sharma28 March 2025 10:30 AM IST
    New Brunswick: Johnson & Johnson MedTech has announced the launch of the DUALTO Energy System, a surgical solution that combines multiple...
    Alexion, AstraZeneca Rare Disease Koselugo gets USFDA nod for neurofibromatosis type 1

    Sanofi gets USFDA fast track designation for Chlamydia vaccine candidate

    Ruchika Sharma27 March 2025 3:22 PM IST
    Paris: Sanofi has received the US Food and Drug Administration (USFDA) fast-track designation for its mRNA vaccine candidate for the...
    USFDA Issues Post-Application Action Letter to Dr Reddys Biologics Unit

    Dr Reddy's Labs, Bio-Thera collaborate for proposed Stelara, Simponi biosimilar

    Ruchika Sharma27 March 2025 2:30 PM IST
    Hyderabad: Dr Reddy's Laboratories SA, wholly-owned subsidiary of Dr Reddy's Laboratories Ltd. and Bio-Thera Solutions, a commercial-stage...
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