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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

    Pfizer Xeljanz secures USFDA nod to treat active ankylosing spondylitis

    Pfizer Xeljanz secures USFDA nod to treat active ankylosing spondylitis

    Ruchika Sharma15 Dec 2021 3:20 PM IST
    New York: Pfizer Inc. has announced that the U.S. Food and Drug Administration (USFDA) has approved the supplemental New Drug Application (sNDA) for...
    Glenmark arm, Almirall ink pact to develop monoclonal antibody for autoimmune diseases

    Glenmark arm, Almirall ink pact to develop monoclonal antibody for autoimmune diseases

    Ruchika Sharma15 Dec 2021 12:52 PM IST
    ISB 880 is a first-in-class fully human, high affinity monoclonal antibody that targets human IL-1RAP.
    Abbott CEO Robert B Ford appointed Chairman of the Board

    Abbott CEO Robert B Ford appointed Chairman of the Board

    Ruchika Sharma14 Dec 2021 11:30 PM IST
    ABBOTT PARK, Ill.: Abbott announced that its Board of Directors has elected Chief Executive Officer Robert B. Ford as Chairman of the Board,...
    Serum Institute plans to launch Novavax shot for children in 6 months

    Serum Institute plans to launch Novavax shot for children in 6 months

    Ruchika Sharma14 Dec 2021 4:39 PM IST
    New Delhi: The Serum Institute of India (SII) plans to launch the Novavax COVID-19 vaccine for children in the country in six months, its CEO said on...
    Dr Reddys bags USFDA nod for VeraRing

    Dr Reddys bags USFDA nod for VeraRing

    Ruchika Sharma14 Dec 2021 3:05 PM IST
    Hyderabad: Drugmaker, Dr Reddy's Labs, has recently announced that the company has received approval from the U.S. Food and Drug Administration...
    Zydus allowed to conduct Phase 2 trial of ZYIL1 in CAPS patients in Australia

    Zydus allowed to conduct Phase 2 trial of ZYIL1 in CAPS patients in Australia

    Ruchika Sharma14 Dec 2021 1:29 PM IST
    Ahmedabad: Global pharmaceutical company, Zydus has announced that it has received permission to initiate the Phase II (a) clinical study of its...
    Lupin gets EIR from USFDA for Goa facility

    Lupin gets EIR from USFDA for Goa facility

    Ruchika Sharma14 Dec 2021 12:13 PM IST
    Mumbai: Global pharma major Lupin Limited today announced that the company has received the Establishment Inspection Report (EIR) from United...
    Moderna to supply additional 20 million COVID vaccine doses to covax

    Moderna to supply additional 20 million COVID vaccine doses to covax

    Ruchika Sharma13 Dec 2021 10:30 PM IST
    Cambridge: Moderna, Inc., has announced an amendment to its existing contract with Gavi, the Vaccine Alliance, to accelerate supply of 20 million...
    Cipla to give nebulisers to primary health care centres in India

    Cipla to give nebulisers to primary health care centres in India

    Ruchika Sharma13 Dec 2021 1:31 PM IST
    New Delhi: Homegrown pharma major Cipla Ltd on Friday said it will donate 5,000 nebulisers to primary health care centres in India as part of its...
    Ahead of IPO, MedPlus raises Rs 418 crore from anchor investors

    Ahead of IPO, MedPlus raises Rs 418 crore from anchor investors

    Ruchika Sharma13 Dec 2021 1:15 PM IST
    New Delhi: Pharmacy retail chain MedPlus Health Services on Friday said it has mobilised Rs 418 crore from anchor investors ahead of its initial share...
    Lupin recalls cartons of oral contraceptive drug Tydemy in US

    Lupin recalls cartons of oral contraceptive drug Tydemy in US

    Ruchika Sharma13 Dec 2021 12:09 PM IST
    The company is recalling the lot due to it being "Subpotent Drug", the US health regulator noted in the report.
    Dr Reddys seeks DCGI nod for Sputnik Light phase 3 trial as booster dose

    Dr Reddys seeks DCGI nod for Sputnik Light phase 3 trial as booster dose

    Ruchika Sharma12 Dec 2021 11:00 AM IST
    New Delhi: Dr Reddy's Laboratories has sought permission from India's drug regulator to conduct a phase-3 clinical trial to evaluate the efficacy and...
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