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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

    Glenmark Pharma Goa facility gets USFDA warning letter

    Glenmark Pharma Goa facility gets USFDA warning letter

    Ruchika Sharma12 Dec 2022 11:33 AM IST
    The US health regulator also pointed out that the company failed to prepare batch production and control records with complete information relating to...
    1.5 lakh Covid vaccine doses procured from Zydus Cadila: Govt

    1.5 lakh Covid vaccine doses procured from Zydus Cadila: Govt

    Ruchika Sharma11 Dec 2022 4:00 PM IST
    New Delhi: A total of 1.5 lakh Covid vaccine doses have been procured by the government from Zydus Cadila at Rs 375.90 per jab (including GST),...
    Lupin Partners with TB Alliance to Advance Telacebec for TB, Leprosy and Buruli Ulcer

    Kite Pharma, Daiichi Sankyo revise YESCARTA CAR T-Cell Therapy licensing agreement

    Ruchika Sharma11 Dec 2022 2:15 PM IST
    Tokyo: Kite Pharma, Inc., a Gilead Company, (hereafter Kite), and Daiichi Sankyo Co., Ltd. have jointly announced the revision of their 2017...
    Janssen-Cilag Guselkumab receives UK nod for Crohns disease, ulcerative colitis

    Janssen seeks USFDA nod for Multiple myeloma treatment Talquetamab

    Ruchika Sharma11 Dec 2022 1:00 PM IST
    Raritan, N.J.: The Janssen Pharmaceutical Companies of Johnson & Johnson has announced the submission of a Biologics License Application...
    Roche bags USFDA nod for companion diagnostic to identify patients with HER2-ultralow metastatic breast cancer eligible for Enhertu

    Roche Alzheimer's disease Cerebrospinal Fluid assays get USFDA clearance

    Ruchika Sharma11 Dec 2022 12:00 PM IST
    The Elecsys AD CSF assays achieve 90% concordance with the Amyloid PET scan imaging.
    Roche bags USFDA nod for companion diagnostic to identify patients with HER2-ultralow metastatic breast cancer eligible for Enhertu

    Roche Diagnostics Middle East secures ISO27001 Information Security certification

    Ruchika Sharma11 Dec 2022 10:00 AM IST
    Dubai: Roche Diagnostics Middle East FZCO has secured the prestigious ISO27001 Information Security certification in recognition of its exceptional...
    Zydus Lifesciences bags USFDA nod for Silodosin, Pregabalin capsules

    Zydus Lifesciences bags USFDA nod for Silodosin, Pregabalin capsules

    Ruchika Sharma10 Dec 2022 2:30 PM IST
    Pregabalin capsules are indicated to treat pain caused by nerve damage due to diabetes or to shingles (herpes zoster) infection.
    AstraZeneca to Invest USD 15 Billion in China by 2030

    Experts say patient selection for AstraZeneca, Daiichi breast cancer drug needs improvement

    Ruchika Sharma10 Dec 2022 1:30 PM IST
    UK: The rush to use AstraZeneca and Daiichi-Sankyo's drug Enhertu to treat certain types of breast cancer has far outpaced doctors' ability to...
    Take action against e-pharmacies for providing predatory pricing: AIOCD tells Niti Ayog

    Take action against e-pharmacies for providing predatory pricing: AIOCD tells Niti Ayog

    Ruchika Sharma10 Dec 2022 12:30 PM IST
    This is nothing but predatory prices and objectives to small pharmacies driving out of the market to create a monopolistic situation, in the long run,...
    Natco Pharma gets 7 USFDA observations for Kothur Pharma Division

    Alembic Pharma gets USFDA EIR for Oncology Injectable Formulation Facility at Panelav

    Ruchika Sharma10 Dec 2022 11:18 AM IST
    Vadodara: Drugmaker Alembic Pharma has recently announced that the Company has received Establishment Inspection Report (EIR) from US Food and Drug...
    Takeda Dengue Tetravalent Vaccine QDENGA gets European Commission nod

    Takeda Dengue Tetravalent Vaccine QDENGA gets European Commission nod

    Ruchika Sharma10 Dec 2022 10:00 AM IST
    QDENGA (TAK-003) is a dengue vaccine that is based on a live-attenuated dengue serotype 2 virus, which provides the genetic “backbone” for all four...
    Lupin, Natco Launch Bosentan Tablets in US With 180-Day Exclusivity

    Lupin unveils generic version of joint pain drug PENNSAID in US

    Ruchika Sharma9 Dec 2022 2:49 PM IST
    Mumbai: Global pharma major Lupin Limited today announced the launch of authorized generic version of PENNSAID (Diclofenac Sodium Topical Solution),...
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