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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

    Bayer Sevabertinib accepted for review in China for advanced non-small cell lung cancer

    Bayer, Puhe BioPharma enter into global license agreement for clinical phase I PRMT5 inhibitor

    Ruchika Sharma27 March 2025 9:15 AM IST
    Berlin: Bayer and Suzhou Puhe BioPharma Co., Ltd., a clinical-stage biotechnology company, have announced that they have entered into a global...
    DoP hosts industry dialogue on Promotion of Research and Innovation in Pharma-MedTech Sector Scheme at Bengaluru

    DoP hosts industry dialogue on Promotion of Research and Innovation in Pharma-MedTech Sector Scheme at Bengaluru

    Ruchika Sharma26 March 2025 5:20 PM IST
    New Delhi: The Department of Pharmaceuticals, Government of India, hosted an Industry Dialogue on the scheme for Promotion of Research and...
    Over 15000 Jan Aushadhi Kendras opened till last month under PMBJP scheme across country: Minister

    Over 15000 Jan Aushadhi Kendras opened till last month under PMBJP scheme across country: Minister

    Ruchika Sharma26 March 2025 4:15 PM IST
    New Delhi: Under the Pradhan Mantri Bhartiya Janaushadhi Pariyojana scheme, a total of 15,057 Jan Aushadhi Kendras (JAKs) have been opened till...
    Dont throw in the bin, please flush it! CDSCO dictum for these 17 medicines

    DoP promotes RnD in Pharma Medtech Sector with AI Integration

    Ruchika Sharma26 March 2025 3:30 PM IST
    New Delhi: The Department of Pharmaceuticals (DoP) has taken steps to promote research and development (R&D) in the sector, including in the areas...
    WHO partners with regulators, experts to strengthen safety and access to medical devices

    WHO collaborates with regulators, experts to strengthen safety, access to medical devices

    Ruchika Sharma26 March 2025 1:15 PM IST
    The five-day workshop, held from 17-21 February in Colombo, focused on advancing the safety, quality, and accessibility of medical devices.
    Granules India appoints Dr PN Baskaran as President - Head API Manufacturing, Operations

    Granules India appoints Dr PN Baskaran as President - Head API Manufacturing, Operations

    Ruchika Sharma26 March 2025 12:35 PM IST
    Telangana: Granules India has announced the appointment of Dr P.N. Baskaran as President - Head API Manufacturing & Operations with effect from...
    GSK Blujepa bags USFDA nod for treatment of uUTIs in female adults, paediatric patients 12 years of age and older

    GSK Blujepa bags USFDA nod for treatment of uUTIs in female adults, paediatric patients 12 years of age and older

    Ruchika Sharma26 March 2025 11:15 AM IST
    London: GSK plc has announced that the Company has received US Food and Drug Administration (FDA) approval for Blujepa (gepotidacin) for the...
    Merck to begin Phase 3 trials for investigational once monthly HIV prevention pill

    Merck gets rights to develop, commercialize Jiangsu Hengrui Pharma heart drug worldwide, excluding Greater China region

    Ruchika Sharma25 March 2025 5:22 PM IST
    The transaction is expected to close in the second quarter of 2025.
    Pune Pharmacist Loses Rs 95 Lakh in Medical Store Deal

    Novo Nordisk, The United Bio-Technology ink pact for 'triple G' obesity drug

    Ruchika Sharma25 March 2025 3:30 PM IST
    China: Novo Nordisk and The United Laboratories International Holdings Limited (TUL)'s wholly-owned subsidiary The United Bio-Technology...
    USFDA approves Abbott Tendyne to replace mitral valve without open-heart surgery

    Abbott begins new Intravascular Lithotripsy trial to improve outcomes in Coronary Artery Disease patients

    Ruchika Sharma25 March 2025 2:30 PM IST
    Abbott Park: Abbott has announced that the U.S. Food and Drug Administration (FDA) has approved an investigational device exemption (IDE) for its...
    GSK application to expand use of Nucala for COPD accepted for review by EMA

    GSK application to expand use of Nucala for COPD accepted for review by EMA

    Ruchika Sharma25 March 2025 1:30 PM IST
    IL-5 is a key cytokine (protein) in type 2 inflammation which is an underlying driver in many diseases.
    Sanofi earns orphan drug designation for multiple myeloma drug

    Sanofi Tolebrutinib under USFDA priority review for multiple sclerosis

    Ruchika Sharma25 March 2025 12:15 PM IST
    Tolebrutinib is currently under clinical investigation, and its safety and efficacy have not been evaluated by any regulatory authority.
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