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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

    Novartis, Argo Biopharma expand strategic alliance with USD 5.2 billion Cardiovascular drugs deal

    Novartis plans to invest USD 23 billion over next 5 years in US based infrastructure

    Ruchika Sharma13 April 2025 12:30 PM IST
    East Hanover: Novartis, a global medicines company, has announced a planned USD 23 billion investment over 5 years in US-based infrastructure,...
    CDSCO Panel Approves Phase IV Protocol Amendment for Bristol-Myers Squibbs Mavacamten Study

    Pomalyst monopoly case: Bristol Myers wins dismissal of lawsuit

    Ruchika Sharma13 April 2025 11:00 AM IST
    A federal judge in New York has dismissed a proposed class action against pharmaceutical giant Bristol Myers Squibb, which accused the company of...
    Morepen Labs plans to employ over 1000 professionals

    Morepen Labs plans to employ over 1000 professionals

    Ruchika Sharma12 April 2025 1:52 PM IST
    Gurugram: Morepen Laboratories Ltd. has announced the addition of more than 1,000 professionals to its salesforce over the next three years,...
    Raid at quack clinic in Telangana, drugs including Amoxycillin seized

    Raid at quack clinic in Telangana, drugs including Amoxycillin seized

    Ruchika Sharma12 April 2025 12:33 PM IST
    Telangana: Drugs Control Administration, Telangana raided a quack's clinic in Medaram Village, Tadvai Mandal, Mulugu District and seized drugs...
    Insufficient Efficacy, Safety Data: CDSCO Panel Rejects Zydus Phase III CT Waiver Request for Voclosporin

    Zydus Lifesciences bags USFDA nod for Duchenne muscular dystrophy drug Jaythari

    Ruchika Sharma12 April 2025 11:30 AM IST
    Ahmedabad: Pharma major, Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (USFDA)...
    USFDA concludes audit at Cohance Lifesciences Jaggaiahpet facility

    Aurobindo Pharma arm gets 11 USFDA observations for Raleigh Plant

    Ruchika Sharma11 April 2025 5:46 PM IST
    Hyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (USFDA) has issued 11 observations after an...
    USFDA plans to phase out animal testing requirement for monoclonal antibodies, other drugs

    USFDA plans to phase out animal testing requirement for monoclonal antibodies, other drugs

    Ruchika Sharma11 April 2025 4:08 PM IST
    In a significant move toward modernizing drug development, the U.S. Food and Drug Administration (USFDA) has announced plans to phase out its...
    Granules India enters high growing peptide segment, CDMO business by acquiring Senn Chemicals

    Granules India successfully closes acquisition of Swiss based CDMO Senn Chemicals

    Ruchika Sharma11 April 2025 3:05 PM IST
    Hyderabad: Granules India Limited has announced the successful closing of the acquisition of Senn Chemicals AG, a Swiss based Contract...
    USFDA approves Tonix Pharma Tonmya for fibromyalgia in adults

    Biocon arm secures USFDA approval for Everolimus Tablets for prophylaxis of organ rejection in adult patients

    Ruchika Sharma11 April 2025 12:30 PM IST
    Bangalore: Biocon Limited has announced that Biocon Pharma Limited, a wholly owned subsidiary of the Company, has received approval...
    Cipla Bommasandra facility gets VAI classification from USFDA

    Cipla gets USFDA nod for Paclitaxel Protein bound Particles for Injectable Suspension

    Ruchika Sharma11 April 2025 11:30 AM IST
    Mumbai: Cipla has announced that the Company has received final approval from the United States Food and Drug Administration (USFDA) for the ...
    Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

    JnJ gets European Commission nod for subcutaneous Darzalex-based quadruplet regimen for newly diagnosed multiple myeloma

    Ruchika Sharma11 April 2025 10:30 AM IST
    Belgium: Janssen-Cilag International NV, a Johnson & Johnson company, has received approval from the European Commission (EC) for an...
    Sanofi India Rodolfo Hrosz resigns as MD

    Sanofi India Rodolfo Hrosz resigns as MD

    Ruchika Sharma10 April 2025 4:11 PM IST
    Mumbai: Sanofi India has announced that Rodolfo Hrosz, Managing Director of the Company, will step down from his current role effective April 30,...
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