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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

    Marksans Pharma UK arm Relonchem gets marketing nod for high BP drug

    Marksans Pharma UK arm Relonchem gets marketing nod for high BP drug

    Ruchika Sharma23 Sept 2025 2:30 PM IST
    Mumbai: Marksans Pharma Limited has announced that its wholly owned subsidiary in UK, Relonchem Limited, has received marketing...
    Intas Pharma appoints Ajay Tiwari as President - HR

    Intas Pharma appoints Ajay Tiwari as President - HR

    Ruchika Sharma23 Sept 2025 1:30 PM IST
    Ahmedabad: Intas Pharma has announced the appointment of Ajay Tiwari as President - Human Resources."Throughout his journey, Ajay has been...
    Shilpa Medicare bags initial authorization for Rotigotine Transdermal Patch from Europe

    Shilpa Medicare gets initial authorization from EMA for Rivaroxaban Orodispersible Films

    Ruchika Sharma23 Sept 2025 12:30 PM IST
    Bengaluru: Shilpa Medicare Limited, headquartered at Raichur, Karnataka, India, has received the initial authorization from European...
    Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

    Dr Reddy's Labs receives positive EMA Committee opinion for proposed biosimilar of Prolia, Xgeva

    Ruchika Sharma23 Sept 2025 11:24 AM IST
    Hyderabad: Dr Reddy's Laboratories Ltd., has announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use...
    CDSCO Panel Recommends Updating Prescribing Information for Sanofis Vaccine

    Sanofi Tolebrutinib faces USFDA review delay; new target action date set for December 28

    Ruchika Sharma22 Sept 2025 5:09 PM IST
    Paris: Sanofi has announced that the US Food and Drug Administration (FDA) has extended by three months the target action date of its review of...
    Show cause notices issued to 196 retail medical shops in Telangana

    115 hospital pharmacies in Telangana receive show cause notices

    Ruchika Sharma22 Sept 2025 4:10 PM IST
    Telangana: A total of 115 pharmacies located in or attached to various corporate hospitals across Telangana have received show cause notices.The Drugs...
    AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

    AstraZeneca-Amgen Tezspire recommended for approval in EU for chronic rhinosinusitis with nasal polyps

    Ruchika Sharma22 Sept 2025 2:00 PM IST
    Cambridge: AstraZeneca and Amgen's Tezspire (tezepelumab) has been recommended for approval in the European Union (EU) for the treatment of adult...
    CII, ICON host strategic dialogue on Indian pharma move toward US manufacturing

    CII, ICON host strategic dialogue on Indian pharma move toward US manufacturing

    Ruchika Sharma22 Sept 2025 1:00 PM IST
    New Delhi: ICON, a US-based construction company in collaboration with the Confederation of Indian Industry (CII ) Telangana, has successfully...
    Medicines worth Rs 50000 seized from quack clinic in Telangana

    Medicines worth Rs 50000 seized from quack clinic in Telangana

    Ruchika Sharma22 Sept 2025 12:00 PM IST
    Telangana: The Drugs Control Administration, Telangana, has uncovered a case of illegal drug stocking following a raid at a quack's clinic in Nagaram...
    Zydus Lifesciences bags USFDA nod for high BP tablet

    Jubilant Pharma arm completes USFDA inspection with zero observations

    Ruchika Sharma22 Sept 2025 11:01 AM IST
    Noida: Jubilant Pharmova Limited has announced the completion of the United States Food and Drug Administration (USFDA) Post-marketing Adverse Drug...
    Himachal cracks down on pharma units, action taken against four facilities

    Zydus gets USFDA EIR for Ahmedabad oncology injectable manufacturing facility

    Ruchika Sharma22 Sept 2025 10:51 AM IST
    Ahmedabad: Zydus has received the Establishment Inspection Report (EIR) from the U.S. Food and Drug Administration (USFDA) for a GMP follow-up...
    Merck Receives Positive EU CHMP Opinion for Expanded Use of Winrevair in Adults with Pulmonary Arterial Hypertension

    Merck receives positive EU CHMP opinion for Enflonsia for RSV in infants

    Ruchika Sharma21 Sept 2025 4:15 PM IST
    Rahway: Merck, known as MSD outside of the United States and Canada,,has announced that the Committee for Medicinal Products for Human Use (CHMP) of...
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