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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

    Biocon Opens First US Manufacturing Facility in New Jersey, Invests USD 30 Million in Expansion

    Biocon Pharma gets USFDA nod for deep vein thrombosis drug Rivaroxaban

    Ruchika Sharma16 May 2025 2:57 PM IST
    Bangalore: Biocon Pharma Limited, a wholly owned subsidiary of Biocon Limited, has received approval for its Abbreviated New Drug...
    Former Coca-Cola executive Punita Lal joins Lupin Board as Additional Director

    Former Coca-Cola executive Punita Lal joins Lupin Board as Additional Director

    Ruchika Sharma16 May 2025 12:59 PM IST
    Mumbai: Global pharma major Lupin Limited has appointed Punita Lal as an Additional Director (Non-Executive, Independent) to its Board of ...
    Lupin Gets Expert Committee Nod To Conduct Phase I Trial of Certolizumab Pegol, IGRA TB Test Made Mandatory

    Lupin Rivaroxaban Tablets approved by USFDA

    Ruchika Sharma16 May 2025 12:23 PM IST
    Mumbai: Global pharma major Lupin Limited has received approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated...
    Alembic Pharma appoints Jigr Shah as Head - Business Finance

    Alembic Pharma appoints Jigr Shah as Head - Business Finance

    Ruchika Sharma16 May 2025 11:30 AM IST
    Vadodara: Alembic Pharma has announced the appointment of Jigr Shah as Head - Business Finance (Senior Management Personnel) of the Company."We...
    Mankind Pharma bags CDSCO nod to start Phase 1 trials of Autoimmune drug candidate

    Mankind Pharma hit with over Rs 341 crore additional tax demand from IT authority

    Ruchika Sharma15 May 2025 5:41 PM IST
    New Delhi: Mankind Pharma Limited has disclosed the receipt of orders from the IT Authority, raising additional tax demands (including interest) of Rs...
    BioNTech to buy CureVac in USD 1.25 billion all-stock deal

    GSK to acquire liver disease drug Efimosfermin for up to USD 2 billion

    Ruchika Sharma15 May 2025 4:10 PM IST
    London: GSK plc and Boston Pharmaceuticals, a clinical stage biopharmaceutical company developing highly targeted therapies for patients with...
    Indoco Remedies arm launches heart attack drug Ticagrelor filmcoated in UK

    USFDA clears Alembic Pharma cardio drug Rivaroxaban, launch expected in next year

    Ruchika Sharma15 May 2025 3:26 PM IST
    Vadodara: Alembic Pharmaceuticals Limited has announced that it has received final approval from the US Food & Drug Administration (USFDA)...
    Unichem Labs Roha facility gets 3 USFDA observations

    USFDA issues EIR for Zydus Lifesciences Ambernath facility

    Ruchika Sharma15 May 2025 1:45 PM IST
    Ahmedabad: Zydus Lifesciences has announced that the company has received the Establishment Inspection Report (EIR) report from...
    Mercks SpringWorks Therapeutics gets nod for Ogsiveo from European Commission for adults with Desmoid Tumors

    After Baclofen, now Gabapentin: Marksans Pharma arm bags another UK MHRA green light

    Ruchika Sharma15 May 2025 12:56 PM IST
    Mumbai: Marksans Pharma Limited has announced that its wholly owned subsidiary in the UK, Relonchem Limited, has received Marketing...
    Merck, Daiichi Sankyo Ifinatamab deruxtecan granted Breakthrough Therapy Designation by USFDA for pretreated extensive-stage small cell lung cancer

    Merck scores USFDA OK for Welireg for 12 years and older with pheochromocytoma or paraganglioma

    Ruchika Sharma15 May 2025 11:45 AM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has received the approval from the U.S. Food and Drug Administration...
    AbbVie completes acquisition of Capstan Therapeutics

    AbbVie Emrelis gets USFDA accelerated approval for a type of lung cancer

    Ruchika Sharma15 May 2025 11:10 AM IST
    North Chicago: AbbVie has received accelerated approval from the U.S. Food and Drug Administration (FDA) for EMRELIS (telisotuzumab...
    Shilpa Medicare Unit VI Bengaluru facility

    Shilpa Pharma Lifesciences Unit 1 gets EIR from USFDA

    Ruchika Sharma15 May 2025 10:15 AM IST
    Karnataka: Shilpa Pharma Lifesciences, a 100% subsidiary of Shilpa Medicare Limited, has received an Establishment Inspection Report...
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