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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

    Senores Pharma to acquire two products of USFDA approved ANDAs from Teva Pharma USA

    AstraZeneca concludes acquisition of Neogene Therapeutics

    Ruchika Sharma17 Jan 2023 1:15 PM IST
    UK: AstraZeneca has completed the acquisition of Neogene Therapeutics Inc.. Neogene will operate as a wholly-owned subsidiary of AstraZeneca, with...
    Roche unveils new PCR test to improve Vaginitis Diagnosis in countries following CE Mark

    Roche gets European Commission nod for Xofluza to treat influenza in children aged one year and above

    Ruchika Sharma17 Jan 2023 12:15 PM IST
    Influenza is a serious infectious disease and represents a significant threat to public health.
    Serum Institute Gets NPPA Nod to Discontinue Two Pack Sizes of Tetanus Toxoid Vaccine

    COVID vaccine: DCGI approves market authorisation for Serum Institute Covovax as heterologous booster dose

    Ruchika Sharma17 Jan 2023 11:14 AM IST
    Covovax is manufactured through technology transfer from Novavax.
    USFDA approves label update for Rybelsus allowing use as first-line option for adults with type 2 diabetes: Novo Nordisk

    USFDA approves label update for Rybelsus allowing use as first-line option for adults with type 2 diabetes: Novo Nordisk

    Ruchika Sharma16 Jan 2023 4:15 PM IST
    Plainsboro: Novo Nordisk has announced that the U.S. Food and Drug Administration (FDA) has approved a label update for Rybelsus (semaglutide) tablets...
    Lupin bags USFDA nod for Dolutegravir, Rilpivirine tablets to treat HIV infection

    Lupin bags USFDA nod for Dolutegravir, Rilpivirine tablets to treat HIV infection

    Ruchika Sharma16 Jan 2023 3:20 PM IST
    Mumbai: Global pharma major Lupin Limited today announced that it has received tentative approval from the United States Food and Drug Administration...
    Solara Active Pharma Sciences Mangalore facility successfully completes USFDA inspection

    USFDA issues 3 observations for Granules India Gagillapur facility

    Ruchika Sharma16 Jan 2023 2:30 PM IST
    Hyderabad: Granules India has recently announced that US Food and Drug Administration (USFDA) has concluded Pre-Approval Inspection (PAI) with three...
    Lupin secures SBTi validation for emission reduction targets

    Lupin gets 2 USFDA observations for Somerset facility

    Ruchika Sharma16 Jan 2023 1:15 PM IST
    Mumbai: Lupin has announced that the company has received two observations from the US Food and Drug Administration (USFDA) at the closure of...
    Zydus Lifesciences arm bags USFDA okay for Major Depressive Disorder drug Levomilnacipran Extended-Release

    Zydus Lifesciences arm bags USFDA okay for Major Depressive Disorder drug Levomilnacipran Extended-Release

    Ruchika Sharma16 Jan 2023 12:15 PM IST
    Ahmedabad: Zydus Lifesciences Limited’s (formerly known as Cadila Healthcare Limited) subsidiary Zydus Pharmaceuticals (USA) Inc. (Zydus) has...
    NPPA Panel Rejects Dr Reddys Omez ODT Plea For Seperate Price, Finds No Therapeutic Edge

    Dr Reddy's Labs acquires trademark rights of breast cancer drug from Pfizer

    Ruchika Sharma16 Jan 2023 11:00 AM IST
    The in-house product will be retailed in the Indian market at a reduction of 85% from the current MRP to increase affordability and access to...
    Cancer MedTech Gets Clarity: CDSCO Releases Final Oncology Device Risk Classification List

    Budget FY24: AiMeD recommends increasing custom duty on import of Chinese medical devices

    Ruchika Sharma15 Jan 2023 1:45 PM IST
    Instead of 18 percent GST applicable on some medical Devices that are not luxury goods, the industry body recommended that the GST needs to be a flat...
    Novartis opens new radioligand therapy manufacturing facility in California

    EMA seeks to issue guidance on liver damage from Novartis gene therapy Zolgensma

    Ruchika Sharma15 Jan 2023 12:15 PM IST
    The drug won conditional EU approval during early 2020 and it costs more than $2 million per patient
    Over 15000 Jan Aushadhi Kendras opened till last month under PMBJP scheme across country: Minister

    Centre approves Pharmaceuticals and Medical Devices Bureau of India proposal to invite online applications for opening Janaushadhi Kendra in 651 districts

    Ruchika Sharma15 Jan 2023 10:00 AM IST
    PMBJP was launched by the Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers with the objective of making quality generic medicines...
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