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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

    Bad Times for Sanofi Healthcare? Market Signals Suggest Growing Pressure

    Sanofi, Cipla collaborate to expand Central Nervous System portfolio reach in India

    Ruchika Sharma28 March 2024 4:48 PM IST
    Mumbai: Sanofi India Limited and Sanofi Healthcare India Private Limited, and Cipla Limited have announced an exclusive partnership for...
    Biocon Gets USFDA Approval for Everolimus Oral Suspension in Pediatric, Adult TSC

    Biocon obtains approval for diabetes drug Liraglutide in UK

    Ruchika Sharma28 March 2024 2:30 PM IST
    Bengaluru: Biocon Limited, a global biopharmaceuticals company, has announced that the Company has received approval from the Medicines and...
    AstraZeneca Gets SEC Nod to Update Lokelma Prescribing Information for Hyperkalemia Treatment

    AstraZeneca India bags dual CDSCO nod for Trastuzumab deruxtecan

    Ruchika Sharma28 March 2024 1:30 PM IST
    Bangalore: AstraZeneca Pharma India Limited has received permission to import for sale and distribution of Trastuzumab deruxtecan lyophilized...
    Zydus

    USFDA inspection: Zydus Lifesciences gets 4 observations for Ahmedabad plant

    Ruchika Sharma28 March 2024 12:30 PM IST
    Ahmedabad: Zydus Lifesciences has announced that the Company has received four observations from the U.S. Food and Drug Administration (USFDA) at...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    USFDA issues ten observations for Alkem Labs Baddi facility

    Ruchika Sharma28 March 2024 11:29 AM IST
    Mumbai: Alkem Labs has announced that the U.S. Food and Drug Administration (USFDA) has issued Form 483 with ten observations at the...
    Advent to Sell Zentiva to Private Equity GTCR in USD 4.8 Billion Deal, Closing Expected in 2026

    Novo Nordisk to acquire Cardior Pharma for up to 1.025 billion Euros

    Ruchika Sharma27 March 2024 1:30 PM IST
    Denmark Novo Nordisk and Cardior Pharmaceuticals have announced that Novo Nordisk has agreed to acquire Cardior for up to 1.025 billion Euros,...
    Johnson and Johnson Agrees to Cut US Drug Prices in Deal with Trump Administration to Avoid Tariffs

    USFDA grants Fast Track designation to JnJ nipocalimab to reduce fetal neonatal alloimmune thrombocytopenia risk in alloimmunized pregnant adults

    Ruchika Sharma27 March 2024 12:30 PM IST
    Spring House: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation (FTD) for...
    USFDA Approves Bionpharmas Generic HIV Drug Etravirine

    Merck gets USFDA nod for WINREVAIR (sotatercept-csrk) for adults with pulmonary arterial hypertension

    Ruchika Sharma27 March 2024 11:51 AM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the U.S. Food and Drug Administration (FDA) has approved...
    Indoco Remedies arm begins commercial production of Pharmaceutical Intermediates

    Indoco Remedies arm begins commercial production of Pharmaceutical Intermediates

    Ruchika Sharma26 March 2024 3:30 PM IST
    Mumbai: Warren Remedies Private Limited, a Wholly Owned Subsidiary of Indoco Remedies Limited has commenced its commercial production from its...
    AstraZeneca Gets SEC Nod to Update Lokelma Prescribing Information for Hyperkalemia Treatment

    AstraZeneca Pharma India names Vinay Sharma as Business Unit Head

    Ruchika Sharma26 March 2024 2:12 PM IST
    Bangalore: AstraZeneca Pharma India Limited has announced the appointment of Vinay Sharma as Business Unit Head - Rare Disease unit with effect...
    AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

    AstraZeneca Ultomiris gets USFDA approval for adults with neuromyelitis optica spectrum disorder

    Ruchika Sharma26 March 2024 12:52 PM IST
    Ultomiris, a long-acting C5 complement inhibitor, provides immediate, complete and sustained complement inhibition.
    Ropanicant Phase-2b trial for Major Depressive Disorder achieves 100 percent enrollment ahead of schedule: Suven Life Sciences

    Bharat Biotech begins clinical trial of Tuberculosis vaccine MTBVAC in India

    Ruchika Sharma26 March 2024 12:34 PM IST
    Hyderabad: Clinical trials of MTBVAC, the Spanish tuberculosis vaccine, the first live attenuated vaccine of Mycobacterium tuberculosis isolated...
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