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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

    Principal Scientific Adviser to GoI reviews progress to transform India regulatory ecosystem for medical products

    Principal Scientific Adviser to GoI reviews progress to transform India regulatory ecosystem for medical products

    Written By Ruchika Sharma22 Aug 2024 11:30 AM IST
    New Delhi: Prof. Ajay Kumar Sood, Principal Scientific Adviser (PSA) to the Government of India took a meeting to review the progress made...
    Daiichi Sankyo, AstraZeneca Enhertu gets USFDA breakthrough therapy designation for certain patients with HER2 low or HER2 ultralow metastatic breast cancer

    Daiichi Sankyo, AstraZeneca Enhertu gets USFDA breakthrough therapy designation for certain patients with HER2 low or HER2 ultralow metastatic breast cancer

    Written By Ruchika Sharma21 Aug 2024 3:37 PM IST
    Tokyo: ENHERTU (fam-trastuzumab deruxtecan-nxki) has been granted Breakthrough Therapy Designation (BTD) in the U.S. for the treatment of unresectable...
    Palamur Biosciences Faces USFDA Warning for Multiple GLP Compliance Failures

    JnJ chemotherapy free lung cancer treatment Rybrevant plus Lazcluze gets USFDA okay

    Written By Ruchika Sharma21 Aug 2024 12:30 PM IST
    New Jersey: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved RYBREVANT (amivantamab-vmjw) plus...
    NPPA Finally Allows GSK to Discontinue Grisovin FP

    GSK secures USFDA Breakthrough Therapy Designation for GSK5764227 for extensive stage small cell lung cancer

    Written By Ruchika Sharma21 Aug 2024 11:30 AM IST
    London: GSK plc has announced that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for GSK5764227 (GSK’227),...
    Johnson and Johnson Agrees to Cut US Drug Prices in Deal with Trump Administration to Avoid Tariffs

    Johnson & Johnson to acquire V-Wave

    Written By Ruchika Sharma21 Aug 2024 10:00 AM IST
    New Brunswick: Johnson & Johnson has announced that it has entered into a definitive agreement to acquire V-Wave Ltd., a privately-held...
    Marksans Pharma Gets USFDA Nod for Generic Tessalon Capsules

    USFDA issues EIR for Marksans Pharma Goa facility

    Written By Ruchika Sharma20 Aug 2024 4:45 PM IST
    Mumbai: Marksans Pharma has announced that the US Food and Drug Administration (USFDA) has issued an Establishment Inspection Report (EIR) for...
    Groundbreaking digital platforms, Indian Pharmacopoeia online portal, Adverse Drug Reaction Monitoring System software launched at First Policy Makers Forum

    Groundbreaking digital platforms, Indian Pharmacopoeia online portal, Adverse Drug Reaction Monitoring System software launched at First Policy Makers' Forum

    Written By Ruchika Sharma20 Aug 2024 12:30 PM IST
    New Delhi: Union Minister of Health and Family Welfare & Chemicals and Fertilizers, Shri J.P. Nadda inaugurated the 'First Policy Makers'...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    Strides Pharma Science arm gets USFDA EIR for Alathur facility

    Written By Ruchika Sharma20 Aug 2024 11:25 AM IST
    Bengaluru: Strides Alathur Private Limited, a wholly-owned subsidiary of Strides Pharma Science Limited has received an Establishment Inspection...
    AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

    AstraZeneca gets USD 107 million Pfizer verdict overturned in US cancer drug patent fight

    Written By Ruchika Sharma19 Aug 2024 4:45 PM IST
    Cambridge: AstraZeneca has convinced a Delaware federal judge to throw out a jury's decision that the company owes USD 107.5 million for...
    Palamur Biosciences Faces USFDA Warning for Multiple GLP Compliance Failures

    USFDA grants marketing authorization for First To Know Syphilis Test for OTC use

    Written By Ruchika Sharma19 Aug 2024 4:00 PM IST
    Springdale: NOWDiagnostics, Inc., a developer of over-the-counter (OTC) and point-of-care (POC) diagnostic tests, has announced that the U.S....
    DCGI Told to Act Against Unapproved Antibiotic FDCs

    India's medicine, antibiotics exports gaining share in US, Italian markets: Govt

    Written By Ruchika Sharma18 Aug 2024 1:15 PM IST
    New Delhi: As the government emphasizes enhancing domestic pharmaceutical manufacturing, India's exports of medicines and antibiotics have begun...
    Imfinzi, Lynparza combo approved in EU for mismatch repair proficient advanced or recurrent endometrial cancer: AstraZeneca

    Imfinzi, Lynparza combo approved in EU for mismatch repair proficient advanced or recurrent endometrial cancer: AstraZeneca

    Written By Ruchika Sharma18 Aug 2024 10:00 AM IST
    Cambridge: AstraZeneca's Imfinzi (durvalumab) and Lynparza (olaparib) have been approved in the European Union (EU) as treatment for certain...
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