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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

    Pfizer Slapped With Rs 8.79 Cr GST Demand Over Alleged ITC Irregularities, Plans Appeal

    Pfizer, BioNTech get USFDA approval, authorization for Omicron KP.2 adapted COVID vaccine

    Ruchika Sharma23 Aug 2024 12:30 PM IST
    New York: Pfizer Inc. and BioNTech SE have announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental Biologics...
    Scheme to strengthen domestic medical device industry to be rolled out in next one month: DoP Secretary

    Scheme to strengthen domestic medical device industry to be rolled out in next one month: DoP Secretary

    Ruchika Sharma23 Aug 2024 11:30 AM IST
    New Delhi: A new scheme will be launched to bolster the domestic medical device industry within next one month, according to Department of...
    Adverse drug reactions from normal saline: Punjab imposes 3-year ban on Captab Biotech

    156 FDCs banned with immediate effect, declared irrational: Ministry of Health and Family Welfare

    Ruchika Sharma22 Aug 2024 6:00 PM IST
    New Delhi: Citing that there is no therapeutic justification for the ingredients contained in fixed dose combinations (FDC) and that the FDC may...
    CDSCO Panel Clears Bristol Myers Yervoy for Two New Cancer Indications

    USFDA accepts application for Opdivo plus Yervoy for unresectable hepatocellular carcinoma

    Ruchika Sharma22 Aug 2024 4:30 PM IST
    Princeton: Bristol Myers Squibb has announced that the U.S. Food and Drug Administration (FDA) has accepted the supplemental Biologics License...
    DMER Releases Pharmacist, Lab Technician CBT Results 2025

    Marksans Pharma subsidiary Relonchem bags marketing authorization from UK MHRA for Fluoxetine Capsules

    Ruchika Sharma22 Aug 2024 3:25 PM IST
    Mumbai: Marksans Pharma Limited has announced that its wholly owned subsidiary Relonchem Limited has received Marketing Authorization from...
    Working on Monkeypox vaccine: Serum Institute CEO

    Working on Monkeypox vaccine: Serum Institute CEO

    Ruchika Sharma22 Aug 2024 1:30 PM IST
    New Delhi: The Serum Institute of India has said that the Company is currently working on developing a Monkeypox vaccine to address the...
    USFDA Approves Bionpharmas Generic HIV Drug Etravirine

    Indoco Remedies secures USFDA nod for Lofexidine Tablets 0.18 mg

    Ruchika Sharma22 Aug 2024 12:30 PM IST
    Mumbai: Indoco Remedies Limited has announced the receipt of final approval from the U.S. Food and Drug Administration (USFDA) for Abbreviated...
    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

    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

    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

    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

    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

    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...
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