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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

    Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

    Nestle India, Dr Reddy's to form JV to bring nutraceutical brands to consumers in India, other agreed territories

    Ruchika Sharma26 April 2024 3:08 PM IST
    The joint venture will help JV Partners combine their strengths and grow their complementary nutraceuticals portfolios in categories such as...
    Pfizer Slapped With Rs 8.79 Cr GST Demand Over Alleged ITC Irregularities, Plans Appeal

    Pfizer Emblaveo gets European Commission marketing nod for patients with multidrug-resistant infections and limited treatment options

    Ruchika Sharma26 April 2024 12:58 PM IST
    New York: Pfizer Inc. has announced that the European Commission (EC) has granted marketing authorization for EMBLAVEO (aztreonam-avibactam) for...
    Lupin Expands GLP-1 Portfolio with Galenicum Semaglutide Deal

    Lupin bags USFDA approval for Loteprednol Etabonate Ophthalmic Suspension

    Ruchika Sharma26 April 2024 11:40 AM IST
    Mumbai: Global pharma major Lupin Limited has announced that the Company has received approval from the United States Food and Drug...
    Granules India packaging facility in US successfully completes USFDA inspection

    Natco Pharma gets USFDA EIR on pharmacovigilance requirements

    Ruchika Sharma25 April 2024 5:44 PM IST
    Telangana: Natco Pharma has informed in a BSE filing that the Company has received the Establishment Inspection Report (EIR) from the US Food and...
    Lupin secures SBTi validation for emission reduction targets

    Lupin Digital Health's Lyfe Platform gets Class C Medical Device license from CDSCO

    Ruchika Sharma25 April 2024 4:23 PM IST
    Mumbai: Lupin Digital Health, India's evidence-based cardiology Digital Therapeutics (DTx) platform, has announced that its Lyfe platform has...
    India targets new markets for pharma export growth amid US tariffs concerns

    Indian pharma exports increase 10 percent to USD 27.9 billion in FY24

    Ruchika Sharma25 April 2024 3:45 PM IST
    New Delhi: In the fiscal year 2023-24, the nation's exports of drugs and pharmaceuticals increased 9.67 per cent year-on-year to USD 27.9...
    NPPA Finally Allows GSK to Discontinue Grisovin FP

    GSK application for expanded indication of Jemperli plus chemotherapy accepted by USFDA for priority review

    Ruchika Sharma25 April 2024 12:40 PM IST
    London: GSK plc has announced the US Food and Drug Administration (FDA) has accepted the supplemental Biologics License Application (sBLA) for...
    USFDA Approves Bionpharmas Generic HIV Drug Etravirine

    Novartis radioligand therapy Lutathera gets USFDA nod for pediatric patients with gastroenteropancreatic neuroendocrine tumors

    Ruchika Sharma25 April 2024 12:14 PM IST
    Basel: Novartis has announced that the U.S. Food and Drug Administration (FDA) has approved Lutathera (USAN: lutetium Lu 177 dotatate / INN:...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    USFDA issues 10 observations for Zydus Lifesciences Jarod facility

    Ruchika Sharma24 April 2024 4:01 PM IST
    Ahmedabad: Zydus Lifesciences has informed in a BSE filing that the US Food and Drug Administration (USFDA) has concluded an inspection with...
    New Drug Application of Zydus Desidustat tablets by China Medical System Holdings accepted in China

    New Drug Application of Zydus Desidustat tablets by China Medical System Holdings accepted in China

    Ruchika Sharma24 April 2024 3:02 PM IST
    Discovered and developed by Zydus, Desidustat is being marketed by the group in India under the brand name Oxemia.
    Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

    Dr Reddy's recalls six lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg over sub potency

    Ruchika Sharma24 April 2024 1:10 PM IST
    Hyderabad, Princeton: Dr Reddy's Laboratories Ltd. has announced that it is voluntarily recalling six (6) lots of Sapropterin...
    Lupin receives positive EMA comittee opinion for eye therapy Ranluspec

    USFDA issues EIR for Lupin Aurangabad facility

    Ruchika Sharma24 April 2024 11:46 AM IST
    Mumbai: Global pharma major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States...
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