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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

    Lupin rolls out Loteprednol Etabonate Ophthalmic Suspension in US

    Lupin rolls out Loteprednol Etabonate Ophthalmic Suspension, 0.5% in US

    Ruchika Sharma16 July 2025 5:04 PM IST
    Mumbai: Global pharma major Lupin Limited has launched Loteprednol Etabonate Ophthalmic Suspension, 0.5%, in the United States,...
    GSK blood cancer drug Blenrep faces USFDA scrutiny over vision issues

    GSK blood cancer drug Blenrep faces USFDA scrutiny over vision issues

    Ruchika Sharma16 July 2025 4:15 PM IST
    GSK's blood cancer drug, Blenrep, is under the U.S. Food and Drug Administration (USFDA) spotlight, as staff reviewers raised safety concerns on...
    Phase 2b trial of Ropanicant

    First patient randomized in Ropanicant Phase 2b trial for Major Depressive Disorder: Suven Life Sciences

    Ruchika Sharma16 July 2025 2:47 PM IST
    Hyderabad: Suven Life Sciences has announced that the first patient has been randomized in its Phase-2b clinical trial evaluating Ropanicant, a...
    Sanofi SAR446597 wins USFDA fast track designation

    Sanofi intravitreal gene therapy wins USFDA fast track designation for geographic atrophy due to age-related macular degeneration

    Ruchika Sharma16 July 2025 1:30 PM IST
    Paris: Sanofi has received fast track designation from the US Food and Drug Administration (FDA) for SAR446597, a one-time intravitreal gene therapy...
    Shilpa Medicare Dabaspet unit gets VAI classification from USFDA

    Shilpa Medicare Dabaspet unit gets VAI classification from USFDA

    Ruchika Sharma16 July 2025 12:14 PM IST
    Karnataka: Shilpa Medicare Limited has received an Establishment Inspection Report (EIR) with Voluntary Action Indicated (VAI)...
    Biocon Biologics expands biosimilar insulin portfolio with USFDA nod of Kirsty

    Biocon Biologics expands biosimilar insulin portfolio with USFDA nod of Kirsty

    Ruchika Sharma16 July 2025 11:30 AM IST
    Karnataka: Biocon Biologics Ltd, a fully integrated global biosimilars company and subsidiary of Biocon Ltd., has received approval...
    Boehringer Ingelheim, LEO Pharma collaborate

    Boehringer Ingelheim, LEO Pharma collaborate to commercialize, further develop Spevigo

    Ruchika Sharma16 July 2025 10:30 AM IST
    Boehringer Ingelheim set to receive EUR 90 million as upfront payment, along with milestone payments and tiered royalties.
    Aurobindo Pharma to manufacture, supply HIV treatment cabotegravir

    Aurobindo Pharma to manufacture, supply HIV treatment cabotegravir across 133 countries

    Ruchika Sharma15 July 2025 5:46 PM IST
    New Delhi: Hyderabad-based drugmaker Aurobindo Pharma will produce and supply Cabotegravir, a long-acting injectable HIV treatment, across 133...
    Zydus Lifesciences bags USFDA okay for arthritis drug Celecoxib

    Zydus Lifesciences bags USFDA okay for Celecoxib Capsules for juvenile rheumatoid arthritis treatment in children

    Ruchika Sharma15 July 2025 5:19 PM IST
    Celecoxib capsules will be produced at Zydus Lifesciences Ltd (SEZ), Ahmedabad.
    Merck to begin Phase 3 trials for investigational once monthly HIV prevention pill

    Merck to begin Phase 3 trials for investigational once monthly HIV prevention pill

    Ruchika Sharma15 July 2025 3:30 PM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has announced the initiation of the EXPrESSIVE Phase 3 clinical trials,...
    GSK blood cancer drug Blenrep faces USFDA scrutiny over vision issues

    GSK application for expanded RSV vaccine Arexvy use for adults 18-49 accepted for review by USFDA

    Ruchika Sharma15 July 2025 2:30 PM IST
    London: GSK plc has announced that the US Food and Drug Administration (FDA) has accepted for review an application to extend the indication of...
    JnJ receives USFDA Approval for updated Varipulse Platform Irrigation Rate

    Johnson & Johnson Medtech bags USFDA approval for updated Varipulse Platform Irrigation Rate

    Ruchika Sharma15 July 2025 1:30 PM IST
    New Brunswick: Johnson & Johnson MedTech has announced the U.S. Food and Drug Administration (FDA) approval of an update to the VARIPULSE...
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