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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

    Indian Pharma market sees 6.9% Growth in May: Report

    Indian Pharma market sees 6.9% growth in May: Report

    Ruchika Sharma19 Jun 2025 3:00 PM IST
    New Delhi: The India pharmaceutical market (IPM) registered a 6.9 percent (on-year) growth in May, primarily propelled by strong performances in...
    Morepen Labs incorporates wholly owned subsidiary in Dubai

    Morepen Labs incorporates wholly owned subsidiary in Dubai

    Ruchika Sharma19 Jun 2025 12:30 PM IST
    Gurugram: Morepen Labs has incorporated a wholly owned subsidiary, MOREPEN LABS - FZCO, in Dubai, United Arab Emirates.The new entity...
    GSK Shingrix approved by USFDA in prefilled syringe presentation

    Gilead Sciences twice-yearly injection for HIV prevention bags USFDA okay

    Ruchika Sharma19 Jun 2025 11:56 AM IST
    Foster City: Gilead Sciences, Inc., a biopharmaceutical company, has received approval from the U.S. Food and Drug Administration (FDA) for...
    Marksans Pharma Oxybutynin hydrochloride 2.5mg/5ml Oral Solution

    Marksans Pharma arm gets marketing authorization for Oxybutynin hydrochloride 2.5mg/5ml Oral Solution in UK

    Ruchika Sharma19 Jun 2025 11:22 AM IST
    Mumbai: Marksans Pharma Limited, an Indian pharmaceutical company, has announced that its wholly owned subsidiary in the...
    Unichem Labs Roha facility gets 3 USFDA observations

    Zydus gets 2 USFDA observations for Ahmedabad oncology injectable site

    Ruchika Sharma19 Jun 2025 10:54 AM IST
    Ahmedabad: Zydus Lifesciences has announced that the US Food and Drug Administration (USFDA) has issued two observations for the...
    Phase 3 trial initiated for Ifinatamab Deruxtecan

    Phase 3 trial initiated for Ifinatamab Deruxtecan in Pretreated Metastatic Castration-Resistant Prostate Cancer: Merck, Daiichi Sankyo

    Ruchika Sharma19 Jun 2025 10:00 AM IST
    Basking Ridge: Merck and Daiichi Sankyo have announced that the first patient has been dosed in the IDeate-Prostate01 phase 3 trial evaluating...
    Govt extends deadline for submitting applications under PLI Scheme

    DoP extends deadline for submitting applications under PLI Scheme for pharma sector

    Ruchika Sharma18 Jun 2025 5:45 PM IST
    New Delhi: The Department of Pharmaceuticals (DoP), Ministry of Chemicals & Fertilizers, has extended the deadline for submitting...
    Alkem Labs appoints Diwakar Gupta as Independent Director

    Diwakar Gupta to join Alkem Labs as Independent Director

    Ruchika Sharma18 Jun 2025 2:33 PM IST
    Maharashtra: Alkem Labs has announced the appointment of Diwakar Gupta as Additional Director designated as an Independent Director on the Board...
    Medtonic to invest nearly Rs 430 crore in new diabetes GCC in Pune

    Medtonic to invest nearly Rs 430 crore in new diabetes GCC in Pune

    Ruchika Sharma18 Jun 2025 2:03 PM IST
    Pune: In a major boost to India's growing healthcare tech scene, global medical device giant Medtronic plc has announced plans to...
    Emcure Pharma Ahmedabad oncology facility concludes USFDA inspection with no observations

    Alembic Pharma gets USFDA EIR for API III facility at Karakhadi

    Ruchika Sharma18 Jun 2025 12:38 PM IST
    Vadodara: Alembic Pharmaceuticals Limited has received Establishment Inspection Report (EIR) from the US Food and Drug Administration (US FDA)...
    JnJ seeks indication extension of Akeega from EMA for adults with metastatic hormone-sensitive prostate cancer, HRR gene alterations

    JnJ seeks USFDA nod of Stelara for pediatric Crohn's disease

    Ruchika Sharma18 Jun 2025 11:58 AM IST
    Horsham: Johnson & Johnson is seeking the U.S. Food and Drug Administration (FDA) approval for the expansion of STELARA (ustekinumab) for the...
    Sanofi successfully prices euro 1.5 billion bond issue

    Sanofi successfully prices euro 1.5 billion bond issue

    Ruchika Sharma18 Jun 2025 10:00 AM IST
    Paris: Sanofi has successfully priced its offering of euro 1.5 billion of notes across 2 tranches:€750 million fixed-rate notes, due June 2029,...
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