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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

    Moderna seeks USFDA nod for Omicron-targeted COVID vaccine for adolescents, children

    Moderna seeks USFDA nod for Omicron-targeted COVID vaccine for adolescents, children

    Ruchika Sharma25 Sept 2022 10:30 AM IST
    US: Moderna Inc said on Friday it has requested U.S. authorization for use of its Omicron-targeting COVID vaccine in adolescents and children.The...
    GSK Nucala application for COPD accepted for review in China

    GSK announces USFDA committee to review Zejula overall survival data from NOVA phase III trial in recurrent ovarian cancer

    Ruchika Sharma24 Sept 2022 5:41 PM IST
    UK: GSK plc has announced that the US Food and Drug Administration (USFDA) will convene a meeting of the Oncologic Drugs Advisory Committee (ODAC) to...
    AstraZeneca, Merck get Chinese nod for Lynparza to treat ovarian cancer

    AstraZeneca, Merck get Chinese nod for Lynparza to treat ovarian cancer

    Ruchika Sharma24 Sept 2022 3:24 PM IST
    In China, Lynparza is approved for the treatment of BRCA-mutated metastatic castration-resistant prostate cancer as well as a 1st-line maintenance...
    Need to fast-track regulatory processes for biotech sector: CII Report

    Need to fast-track regulatory processes for biotech sector: CII Report

    Ruchika Sharma24 Sept 2022 12:15 PM IST
    "There is a need for autonomy in policy making and implementation," the report released on Friday at the 4th CII Lifesciences Conclave stated.
    Cipla gets USFDA EIR for Indore facility

    Cipla gets USFDA EIR for Indore facility

    Ruchika Sharma24 Sept 2022 11:07 AM IST
    Mumbai: Pharma major, Cipla, has recently announced that the Company has received Establishment Inspection Report (EIR) from the United States Food...
    Low-Risk Medical Device Makers Get Clarity: CDSCO Publishes Class A Risk Classification List under MDR 2017

    Govt approves setting up of Exports Promotion Council for Medical Devices

    Ruchika Sharma23 Sept 2022 5:00 PM IST
    The new Export Promotion Council (EPC) for medical devices will be set up, with Headquarters in YEIDA, Greater Noida, Uttar Pradesh, and regional...
    USFDA nod to Eli Lilly RET Inhibitor Retevmo for adults with advanced or metastatic solid tumors with a RET Gene Fusion, regardless of type

    USFDA nod to Eli Lilly RET Inhibitor Retevmo for adults with advanced or metastatic solid tumors with a RET Gene Fusion, regardless of type

    Ruchika Sharma23 Sept 2022 4:20 PM IST
    In addition to the tumor-agnostic approval, the USFDA has granted traditional approval for Retevmo in adult patients with locally advanced or...
    Aurobindo Pharma US arm gets USFDA EIR for Raleigh facility

    Aurobindo Pharma US arm gets USFDA EIR for Raleigh facility

    Ruchika Sharma23 Sept 2022 2:32 PM IST
    Hyderabad: Aurobindo Pharma has recently announced that Aurolife Pharma LLC, a wholly owned step-down subsidiary of the Company has received an...
    Shilpa Medicare Hyderabad division gets USFDA clearance

    Shilpa Medicare Hyderabad division gets USFDA clearance

    Ruchika Sharma23 Sept 2022 12:15 PM IST
    The USFDA clearance on the facility will enable the company to test and release batches into the US from this facility.
    Lupin bags USFDA nod for Diclofenac Sodium Topical Solution to treat arthritic knee pain

    Lupin bags USFDA nod for Diclofenac Sodium Topical Solution to treat arthritic knee pain

    Ruchika Sharma23 Sept 2022 11:15 AM IST
    The product will be manufactured at Lupin's facility in Pithampur, India.
    COVID-19 Treatment: GSK Sotrovimab, Roche antibody cocktail casirivimab-imdevimab no longer recommended by WHO

    COVID-19 Treatment: GSK Sotrovimab, Roche antibody cocktail casirivimab-imdevimab no longer recommended by WHO

    Ruchika Sharma22 Sept 2022 4:14 PM IST
    Both therapies continue to be recommended for use by the European drugs regulator.
    Novartis intrathecal onasemnogene abeparvovec Phase III study

    Novartis to take US drug patent case to Supreme Court

    Ruchika Sharma22 Sept 2022 3:46 PM IST
    Zurich: Novartis AG plans to ask the U.S. Supreme court to uphold the validity of a patent it holds on the dosing regimen for multiple sclerosis drug...
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