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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

    Shilpa Medicare gets initial authorization from EMA for Rivaroxaban Orodispersible Films

    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 receives positive EMA Committee opinion for proposed biosimilar of Prolia, Xgeva

    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...
    Toxic Coldrif Fallout: Tamil Nadu Govt Issues Show-Cause Notice to Sresan Pharma, License at Risk

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

    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...
    Lupin gets USFDA OAI status for Pithampur Unit 2 facility

    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...
    Coldrif Fallout: How a Pharma firm skipped Indias Drug Watchdog inspections

    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 Enflonsia for RSV in infants -stage small cell lung cancer

    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...
    Roche receives CE mark for AI based Kidney Klinrisk Algorithm

    Roche subcutaneous formulation of Lunsumio recommended by CHMP for EU nod for follicular lymphoma

    Ruchika Sharma21 Sept 2025 2:45 PM IST
    Basel: Roche has announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of...
    Bayer new drug application for gadoquatrane accepted for review in China

    Bayer new drug application for gadoquatrane accepted for review in China

    Ruchika Sharma21 Sept 2025 2:00 PM IST
    Berlin: Bayer today announced that the Center of Drug Evaluation of China's National Medical Products Administration has accepted the new drug...
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