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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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    Articles By : Ruchika Sharma

    Lupin Receives USFDA EIR with VAI Status for Goa Manufacturing Plant

    Lupin bags tentative USFDA nod for Raltegravir Tablets for HIV-1 infection

    Written By Ruchika Sharma9 Nov 2024 11:00 AM IST
    Mumbai: Global pharma major Lupin Limited has announced that the Company has received tentative approval from the United States Food and Drug...
    USFDA Approves Johnson and Johnson Blood Cancer Drug Tecvayli-Darzalex Combo

    Johnson & Johnson MedTech bags USFDA nod for the Varipulse Pulsed Field Ablation Platform for atrial fibrillation

    Written By Ruchika Sharma8 Nov 2024 11:00 AM IST
    Irvine: Johnson & Johnson MedTech has announced the U.S. Food & Drug Administration (FDA) approval of the VARIPULSE Platform for the...
    Boehringer Ingelheims Vetmedin Becomes First USFDA-Approved Drug to Delay Heart Failure in Dogs

    Boehringer Ingelheim, Broad Institute of MIT and Harvard to develop treatments for people with mental health conditions

    Written By Ruchika Sharma8 Nov 2024 9:00 AM IST
    Ingelheim: Boehringer Ingelheim and researchers from the Stanley Center for Psychiatric Research at the Broad Institute of MIT and Harvard have agreed...
    Sanofis Sarclisa Gets EMA Nod for Subcutaneous On-Body Injector Version

    Sanofi, Regeneron Dupixent approved in EU for young children with eosinophilic esophagitis

    Written By Ruchika Sharma7 Nov 2024 3:55 PM IST
    Paris: Sanofi has announced that the European Medicines Agency has approved Dupixent (dupilumab) to treat eosinophilic esophagitis (EoE) in...
    NCLT Chennai Approves Apollo Hospitals’ Composite Scheme of Arrangement

    Apollo Hospitals exceeds Q2 profit forecast on strong demand for healthcare services

    Written By Ruchika Sharma7 Nov 2024 11:30 AM IST
    Bengaluru: Apollo Hospitals Enterprise exceeded profit expectations for the second quarter, with increased demand for healthcare services driving...
    Venus Remedies expands presence in Vietnam with marketing nods for Methotrexate, Cefuroxime, Irinotecan

    Venus Remedies expands reach in ASEAN region with Malaysian PIC/S GMP nod for Pre-filled Syringe facility

    Written By Ruchika Sharma5 Nov 2024 3:30 PM IST
    Mumbai: Venus Remedies Limited, a exporter of generic drugs with presence in more than 80 countries, has received Good Manufacturing...
    Dr Reddy gets CDSCO Panel nod for oral semaglutide

    Dr Reddy's Labs recalls over 3 lakh bottles of Cinacalcet tablets in US over manufacturing issues

    Written By Ruchika Sharma5 Nov 2024 1:30 PM IST
    New Delhi: Dr Reddy's Laboratories is recalling over 3.3 lakh bottles of Cinacalcet tablets, a medication used for treatment of high calcium...
    Health Ministry Appoints 27 Government Analysts as Medical Device Testing Officers

    Natco Pharma names Imtiyaz Basade as Senior Vice President - RAD, Pharma Division, Kothur Unit

    Written By Ruchika Sharma5 Nov 2024 11:24 AM IST
    Telangana: Natco Pharma has announced that Imtiyaz Basade has been appointed as Senior Vice President - RAD, Pharma Division, Kothur Unit w.e.f....
    Shilpa Medicare bags initial authorization for Rotigotine Transdermal Patch from Europe

    Shilpa Medicare gets four USFDA observations for Bengaluru facility

    Written By Ruchika Sharma4 Nov 2024 3:58 PM IST
    Raichur: Shilpa Medicare has announced that the US Food and Drug Administration (USFDA) has issued Form 483 with four observations at the...
    Ciplas Lanreotide Supply Partners Greece Plant Gets USFDA OAI Status

    USFDA classifies Cipla Goa facility as VAI

    Written By Ruchika Sharma4 Nov 2024 11:30 AM IST
    Mumbai: Through a recent BSE filing, Cipla has informed that the United States Food and Drug Administration (USFDA) has classified the routine...
    Lupin Receives USFDA EIR with VAI Status for Goa Manufacturing Plant

    Lupin to focus on development of inhalers with near-zero global warming potential propellants

    Written By Ruchika Sharma3 Nov 2024 11:00 AM IST
    Mumbai: Global pharma major Lupin Limited has announced its focus on formulating respiratory inhalers by incorporating a propellant with...
    Merck

    Merck, Moderna begin Phase 3 Trial of V940 with Keytruda in non small lung cancer

    Written By Ruchika Sharma3 Nov 2024 10:00 AM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, and Moderna, Inc., announced the initiation of INTerpath-009, a pivotal...
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