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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

    Tamil Nadu cancels licence of Sresan Pharma, orders shutdown

    Licences of 2 pharma stores suspended for unethical trade practices

    Ruchika Sharma26 July 2025 12:30 PM IST
    Jammu: In continuation to its efforts to curb the unlawful distribution and misuse of habit-forming drugs, Drugs & Food Control Organisation...
    Goa unveils lifesaving therapies pricing policy

    16912 Jan Aushadhi Kendras opened till June 30: Minister

    Ruchika Sharma26 July 2025 11:30 AM IST
    New Delhi: The Government launched the Pradhan Mantri Bhartiya Janaushadhi Pariyojana scheme to make quality generic medicines available at...
    Delhi ITAT Deletes Rs 14.98 Cr Ad-Hoc Disallowance on Mankind Pharmas Travel Expenses

    Mankind Pharma incorporates wholly owned subsidiary in Sri Lanka

    Ruchika Sharma26 July 2025 10:00 AM IST
    New Delhi: Mankind Pharma has announced the incorporation of a wholly owned subsidiary in Sri Lanka under the name and style of Mankind Pharma...
    Dr Reddys Labs receives positive EMA Committee opinion for proposed biosimilar of Prolia, Xgeva

    Dr Reddy's Labs plans to roll out cheaper Wegovy copycat across 87 countries in 2026: CEO

    Ruchika Sharma25 July 2025 4:30 PM IST
    Hyderabad: Dr. Reddy's Laboratories is gearing up to shake up the global weight-loss drug market with the launch of an affordable copycat version...
    Action taken against 694 manufacturing units since 2022: Minister

    Action taken against 694 manufacturing units since 2022: Minister

    Ruchika Sharma25 July 2025 2:30 PM IST
    New Delhi: Actions have been taken against 694 drug manufacturing units following the inspections at 905 firm units since 2022, the...
    European Commission approves indication extension of JnJ Imbruvica in frontline mantle cell lymphoma

    J&J Imbruvica gains EU approval for untreated Mantle Cell Lymphoma in transplant eligible patients

    Ruchika Sharma25 July 2025 12:40 PM IST
    Beerse: Janssen-Cilag International NV, a Johnson & Johnson company, has announced that the European Commission (EC) has approved an...
    Tata 1mg in Advanced Talks to Raise USD 200 Million, Valuation Standoff Emerges

    Shilpa Medicare arm to infuse USD 2 million in Alveolus Bio

    Ruchika Sharma25 July 2025 12:13 PM IST
    Raichur: Shilpa Medicare has announced that Shilpa Pharma Inc, a wholly owned subsidiary of the company, will make a strategic...
    Natco Pharma gets USFDA EIR for Kothur Pharma division

    Natco Pharma Mekaguda API unit gets USFDA EIR

    Ruchika Sharma24 July 2025 3:46 PM IST
    Hyderabad: NATCO Pharma Limited has announced that the U.S. Food and Drug Administration (USFDA) has issued an Establishment Inspection...
    Zydus Gets CDSCO Panel Nod to Market Sodium Chloride Nebuliser Solution

    Zydus Lifesciences receives tentative approval from USFDA for Chronic lymphocytic leukaemia drug Ibrutinib

    Ruchika Sharma24 July 2025 3:24 PM IST
    Ahmedabad: Zydus Lifesciences Limited has announced that it has received tentative approval from the United States Food and Drug Administration...
    Roche Itovebi gets European Commission nod

    Roche Itovebi gets European Commission nod in fight against advanced breast cancer

    Ruchika Sharma24 July 2025 2:30 PM IST
    Basel: Roche has received approval from the European Commission for Itovebi (inavolisib), in combination with palbociclib (Ibrance) and...
    GSK Gepotidacin approved in UK for UTIs in females aged 12 years and older

    USFDA extends review period for GSK Blenrep in relapsed/refractory multiple myeloma

    Ruchika Sharma24 July 2025 1:30 PM IST
    London: GSK plc has announced the extension of the US Food and Drug Administration (FDA) review period for the Biologics License Application...
    JnJ gets positive CHMP opinion of nipocalimab for antibody-positive patients living with generalised myasthenia gravis

    JnJ Darzalex gets European Commission nod for high-risk smouldering multiple myeloma

    Ruchika Sharma24 July 2025 12:15 PM IST
    Beerse: Janssen-Cilag International NV, a Johnson & Johnson company, has received approval from the European Commission (EC) for a new...
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