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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

    Merck gets USFDA Priority Review for application for Keytruda plus standard of care as Perioperative treatment for Resectable Locally Advanced Head, Neck Squamous Cell Carcinoma

    Merck announces Phase 3 trial initiations for 4 investigational candidates from its hematology, oncology pipeline

    Ruchika Sharma6 Jan 2024 12:30 PM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has announced the initiation of pivotal Phase 3 trials for four of its...
    Import Nod on Hold Over False Positives, Tissue Detection: CDSCO Panel Seeks More Data on Medtronics PTeye Device

    Medtronic gets CE Mark for next generation Micra leadless pacing systems

    Ruchika Sharma6 Jan 2024 11:32 AM IST
    Medtronic projects the battery life of Micra AV2 and Micra VR2 is nearly 16 and 17 years, respectively.
    GSK, Pfizer resolve patent lawsuit over RSV vaccines

    Botox rival Revance loses bid to dismiss Allergan trade secrets lawsuit

    Ruchika Sharma5 Jan 2024 4:15 PM IST
    United States: A federal judge on Wednesday said Botox maker AbbVie's Allergan unit can move ahead with its lawsuit accusing Revance...
    Merck gets USFDA Priority Review for application for Keytruda plus standard of care as Perioperative treatment for Resectable Locally Advanced Head, Neck Squamous Cell Carcinoma

    Merck seeks GLP-1 drugs with benefits beyond weight loss, says CEO

    Ruchika Sharma5 Jan 2024 3:36 PM IST
    Rahway: Merck & Co is seeking GLP-1 treatments with benefits beyond weight loss, CEO Robert Davis said on Thursday at a conference.Newer...
    Dr Reddys Labs inks pact with Henlius for commercialization of multiple myeloma injection HLX15 in US, Europe

    Dr Reddy's Labs acquires entire MenoLabs supplements portfolio

    Ruchika Sharma5 Jan 2024 1:30 PM IST
    Brands include MenoFit and MenoGlow probiotics, Happy Fiber and Well Rested dietary supplements, Athena's Shield menopause support supplement, and...
    Revenue of 25 leading domestic pharma cos expected to grow 9-11 percent in current fiscal year: ICRA

    Revenue of 25 leading domestic pharma cos expected to grow 9-11 percent in current fiscal year: ICRA

    Ruchika Sharma5 Jan 2024 12:30 PM IST
    New Delhi: Revenue of 25 leading domestic pharmaceutical companies is expected to grow 9-11 per cent in the current fiscal year, as per Icra.The...
    Lupin bags tentative USFDA nod for Dapagliflozin and Saxagliptin Tablets

    Lupin bags tentative USFDA nod for Dapagliflozin and Saxagliptin Tablets

    Ruchika Sharma5 Jan 2024 11:11 AM IST
    Dapagliflozin and Saxagliptin Tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes...
    Esperion, Daiichi Sankyo Europe announce USD 125 million amendment to their collaboration, including resolution of pending litigation

    Esperion, Daiichi Sankyo Europe announce USD 125 million amendment to their collaboration, including resolution of pending litigation

    Ruchika Sharma4 Jan 2024 4:45 PM IST
    Ann Arbor: Esperion Therapeutics, Inc. and Daiichi Sankyo Europe GmbH (DSE), the European headquarter organization of the Japanese pharmaceutical...
    Natco Pharma net profit down 23.44 percent at Rs 517.9 crore in Q2

    Natco Pharma concludes transition of DASH Pharma into Natco Pharma USA

    Ruchika Sharma4 Jan 2024 3:42 PM IST
    Parsippany: Natco Pharma Limited, a research and development (R&D)-focused pharmaceutical company based in India, has announced that DASH...
    Bristol Myers Squibb Breyanzi approved by USFDA for adults with Marginal Zone Lymphoma

    Bristol Myers Squibb Repotrectinib application to treat cancer validated by EMA

    Ruchika Sharma4 Jan 2024 1:30 PM IST
    Princeton: Bristol Myers Squibb has announced that the European Medicines Agency (EMA) has validated its marketing authorization application...
    Genmab, AbbVie Face Setback as Epcoritamab Misses Survival Goal in Lymphoma Study

    CVS Health to remove AbbVie rheumatoid arthritis drug Humira from some drug reimbursement lists in April

    Ruchika Sharma4 Jan 2024 12:30 PM IST
    A CVS spokesperson said the company expects most of its customers to transition their coverage to biosimilars of Humira, known chemically as...
    Pfizer Sells ViiV Stake for USD 1.9 Billion, Shionogi Emerges Bigger Partner

    Pfizer gene therapy for bleeding disorder approved in Canada

    Ruchika Sharma4 Jan 2024 11:51 AM IST
    Canada: Pfizer said on Wednesday that Canada's health regulator approved its gene therapy for the treatment of a rare inherited bleeding...
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