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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 [email protected] Contact no. 011-43720751

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    Articles By : Ruchika Sharma

    Boehringer Ingelheims Vetmedin Becomes First USFDA-Approved Drug to Delay Heart Failure in Dogs

    Boehringer Ingelheim, Sosei Heptares collaborate to develop first-in-class treatments targeting all symptoms of schizophrenia

    Written By Ruchika Sharma11 March 2024 9:00 AM IST
    Ingelheim: Boehringer Ingelheim and Sosei Group Corporation have announced they have entered a global collaboration and exclusive...
    USFDA Approves Eli Lillys Weight-Loss Pill Foundayo, Intensifies Rivalry with Novo Nordisk

    USFDA delays decision on Eli Lilly Alzheimer's drug Donanemab

    Written By Ruchika Sharma10 March 2024 4:30 PM IST
    White said the FDA wants the expert panel to discuss some of the unique aspects of the clinical trial used in its request for a traditional FDA...
    Pill form of Wegovy gets USFDA approval for weight loss

    Working with several countries authorities to tackle counterfeit versions of Ozempic: Novo Nordisk CEO

    Written By Ruchika Sharma10 March 2024 12:15 PM IST
    Denmark: Novo Nordisk's CEO on Friday said the company was working with authorities in several countries to tackle counterfeit versions of its popular...
    Pill form of Wegovy gets USFDA approval for weight loss

    Novo Nordisk Wegovy gets USFDA nod for lowering heart risks

    Written By Ruchika Sharma9 March 2024 2:30 PM IST
    Denmark: Novo Nordisk has announced that the US Food and Drug Administration (FDA) has approved a label expansion for Wegovy based on a...
    CDSCO Panel Clears Bristol Myers Yervoy for Two New Cancer Indications

    USFDA approves Opdivo in combo with Cisplatin and Gemcitabine for first-line treatment of adult patients with metastatic Urothelial Carcinoma: Bristol Myers Squibb

    Written By Ruchika Sharma9 March 2024 1:30 PM IST
    Princeton: Bristol Myers Squibb has announced that the U.S. Food and Drug Administration (FDA) approved Opdivo (nivolumab), in combination...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    Alembic Pharma gets 4 USFDA observations for Panelav facility

    Written By Ruchika Sharma9 March 2024 12:30 PM IST
    Vadodara: Alembic Pharma has announced that the Company has received a Form 483 with four procedural observations from the United States...
    Cipla Recalls Cancer Drug Nilotinib in US Over Manufacturing Issue

    Sun Pharma unit recalls over 54000 bottles of Mesalamine ER capsules in US

    Written By Ruchika Sharma9 March 2024 11:24 AM IST
    The affected lot of capsules have been manufactured by Sun Pharmaceutical Industries at its Mohali-based manufacturing plant and distributed in the US...
    USFDA Approves Eli Lillys Weight-Loss Pill Foundayo, Intensifies Rivalry with Novo Nordisk

    Eli Lilly finds bacteria, other impurities in Mounjaro, Zepbound knockoffs

    Written By Ruchika Sharma8 March 2024 5:48 PM IST
    Eli Lilly said on Thursday it has found bacteria and high levels of impurities in products claiming to be compounded versions of tirzepatide, the...
    Johnson and Johnson Agrees to Cut US Drug Prices in Deal with Trump Administration to Avoid Tariffs

    Latest JnJ talc trial ends with hung jury

    Written By Ruchika Sharma8 March 2024 1:30 PM IST
    New York: The latest trial over claims that Johnson & Johnson's talc products cause cancer ended in a mistrial on Tuesday, as a Florida state...
    Granules India packaging facility in US successfully completes USFDA inspection

    USFDA gives nod for commercial production at Zydus Ahmedabad API unit

    Written By Ruchika Sharma7 March 2024 5:07 PM IST
    Ahmedabad: Pharma major Zydus Lifesciences has announced that the company has received Post Application Action Letter from the US Food and...
    Chalk powder instead of medicines: Telangana drug controller issues alert against drugs by Meg Lifesciences

    Chalk powder instead of medicines: Telangana drug controller issues alert against drugs by Meg Lifesciences

    Written By Ruchika Sharma7 March 2024 4:31 PM IST
    Telangana: In a significant move to curb the menace of falsified drugs, the Drugs Control Administration, Telangana, has issued a Spurious Drug Alert...
    Bristol Myers Squibb Wins USFDA Approval for Opdivo Combo in Hodgkin Lymphoma

    Boehringer Ingelheim accused of misusing US patents to delay asthma-drug rivals

    Written By Ruchika Sharma7 March 2024 12:38 PM IST
    German drugmaker Boehringer Ingelheim was accused in a federal lawsuit in Boston on Wednesday of improperly submitting patents to the U.S. Food and...
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