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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

    Granules India honoured with Golden Peacock Award for Sustainability

    Granules India honoured with Golden Peacock Award for Sustainability

    Ruchika Sharma15 Nov 2024 11:00 AM IST
    Hyderabad: Granules India Limited, a pharmaceutical company, has announced that it has received the Golden Peacock Award for Sustainability....
    AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

    AstraZeneca, Daiichi Sankyo submits Datopotamab deruxtecan new BLA for accelerated approval in US for lung cancer

    Ruchika Sharma14 Nov 2024 3:15 PM IST
    AstraZeneca and Daiichi Sankyo have submitted a new Biologics License Application (BLA) for accelerated approval in the US for datopotamab deruxtecan...
    CDSCO Panel Approves GSKs Proposal to Double Indian Patient Pool in Dostarlimab Trial

    GSK Ojjaara approved in Canada for treatment of myelofibrosis in adults who have moderate to severe anemia

    Ruchika Sharma14 Nov 2024 1:15 PM IST
    Mississauga: GSK has announced that Health Canada has approved Ojjaara (momelotinib) for the treatment of splenomegaly and/or...
    Eli Lilly Collaborates with Laekna to Develop Obesity Drug Targeting Muscle Preservation and Weight Loss

    Ginkgo Bioworks advances collaboration with Merck to improve Biologics manufacturing

    Ruchika Sharma14 Nov 2024 12:33 PM IST
    Boston: Ginkgo Bioworks has announced the completion of the first milestone of a previously announced partnership with Merck, known as MSD outside of...
    Granules India arm gets 1 USFDA observation for Hyderabad facility

    Cipla gets 8 USFDA observations for Virgonagar facility

    Ruchika Sharma14 Nov 2024 12:01 PM IST
    Mumbai: Cipla has announced that the United States Food and Drugs Administration (USFDA) has concluded an inspection at the Company's...
    Natco Pharma net profit jumps 83 percent to Rs 676 crore in Q2

    Natco Pharma net profit jumps 83 percent to Rs 676 crore in Q2

    Ruchika Sharma13 Nov 2024 5:21 PM IST
    Natco Pharma has announced an 83 percent on-year increase in its consolidated net profit for the September 2024 quarter, which rose to Rs 676 crore,...
    Shanghai Pharma Vice President expresses hope for increased investment from Indian pharma cos in China

    Shanghai Pharma Vice President expresses hope for increased investment from Indian pharma cos in China

    Ruchika Sharma13 Nov 2024 2:25 PM IST
    Shanghai: Li Dongming, Vice President of Shanghai Pharmaceuticals, expressed hope on Tuesday for more investment from Indian pharmaceutical...
    USFDA Suspends Ixchiq Chikungunya Vaccine License Citing Encephalitis Death, 20+ Serious Adverse Events

    USFDA accepts Shilpa Medicare CDMO partner Unicycive NDA for Oxylanthanum Carbonate

    Ruchika Sharma13 Nov 2024 12:13 PM IST
    Karnataka: Shilpa Medicare CDMO partner Unicycive Therapeutics, Inc. has announced that the U.S. Food and Drug Administration (USFDA) has...
    Aurobindo Pharma in lead to acquire Zentiva for US 5.5 billion: ET Report

    Aurobindo Pharma arm gets GMP certificate of compliance for biosimilars manufacturing facility from EMA

    Ruchika Sharma13 Nov 2024 11:45 AM IST
    Hyderabad: CuraTeQ Biologics Private Limited, a wholly owned subsidiary of Aurobindo Pharma Limited, has received a GMP certificate of...
    Jubilant Pharmova to sell API business to wholly owned arm

    Alembic Pharma bags USFDA nod for Ivabradine Tablets

    Ruchika Sharma12 Nov 2024 4:05 PM IST
    Vadodara: Alembic Pharmaceuticals Limited has announced that it has received Final Approval from the US Food & Drug Administration (USFDA) for...
    AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

    USFDA grants Breakthrough Therapy Designation to Nipocalimab for treatment of adults with moderate-to-severe Sjögren's disease: JnJ

    Ruchika Sharma12 Nov 2024 1:00 PM IST
    Spring House: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has granted nipocalimab Breakthrough Therapy...
    USFDA removes clinical hold on Novavax COVID Influenza combination, stand alone Influenza Phase 3 trial

    USFDA removes clinical hold on Novavax COVID Influenza combination, stand alone Influenza Phase 3 trial

    Ruchika Sharma12 Nov 2024 11:00 AM IST
    Gaithersburg: Novavax, Inc., a global company advancing protein-based vaccines with its Matrix-M adjuvant, has announced that the U.S. Food and...
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