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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

    Granules India packaging facility in US successfully completes USFDA inspection

    USFDA inspection: Biocon gets 4 observations for Visakhapatnam API facility

    Ruchika Sharma24 Jun 2024 2:15 PM IST
    Bangalore: Biocon has informed in a BSE filing that the U.S. Food and Drug Administration (USFDA) has concluded a GMP inspection of the...
    Sun Pharma Launches UNLOXCYT for Advanced Skin Cancer in US

    Sun Pharma GL0034 demonstrates significant weight loss, gluco-metabolic and lipid lowering efficacy in individuals with obesity in oral presentation

    Ruchika Sharma24 Jun 2024 1:30 PM IST
    Mumbai: Sun Pharmaceutical Industries Limited has announced results from a Phase 1, multiple ascending-dose study evaluating the safety,...
    Biocon Gets USFDA Approval for Everolimus Oral Suspension in Pediatric, Adult TSC

    Biocon arm receives EMA approval to manufacture biosimilar Bevacizumab at Bengaluru facility

    Ruchika Sharma24 Jun 2024 12:15 PM IST
    Bengaluru: Biocon Biologics Ltd, a global, fully integrated biosimilars company and a subsidiary of Biocon Ltd, has received approval from the...
    Lupin Expands GLP-1 Portfolio with Galenicum Semaglutide Deal

    USFDA issues EIR for Lupin Somerset facility

    Ruchika Sharma24 Jun 2024 11:18 AM IST
    Mumbai: Global pharma major Lupin Limited today announced that it has received the Establishment Inspection Report (EIR) from the United States...
    Roche Lunsumio VELO bags USFDA approval for subcutaneous use in follicular lymphoma

    Roche gets USFDA nod for chronic blood disorder treatment Crovalimab

    Ruchika Sharma23 Jun 2024 4:30 PM IST
    Roche has received approval from the U.S. Food and Drug Administration (USFDA) for Crovalimab for the treatment of chronic blood...
    JnJ completes acquisition of Halda Therapeutics, its novel platform for cancer treatment

    JnJ completes acquisition of Proteologix

    Ruchika Sharma23 Jun 2024 1:30 PM IST
    New Brunswick: Johnson & Johnson has announced that it has successfully completed the acquisition of Proteologix, Inc., a privately-held...
    Takeda announces closing of partnership with Innovent Biologics for oncology medicines

    Takeda gets European Commission approval for Fruzaqla for previously treated metastatic Colorectal cancer

    Ruchika Sharma23 Jun 2024 12:00 PM IST
    FRUZAQLA is a selective oral inhibitor of all three VEGF receptors (-1, -2 and -3). VEGFR inhibitors play a pivotal role in blocking tumor...
    CDSCO Panel Clears Bristol Myers Yervoy for Two New Cancer Indications

    Bristol Myers Squibb application for subcutaneous Nivolumab validated by EMA

    Ruchika Sharma23 Jun 2024 10:00 AM IST
    Princeton: Bristol Myers Squibb has announced that the European Medicines Agency (EMA) has validated the extension application to introduce...
    USFDA Flags Sarfez Pharma for Misleading Promotion of Torsemide Drug Soaanz

    WHO, Eli Lilly warn against fake versions of popular weight loss, diabetes drugs

    Ruchika Sharma22 Jun 2024 4:46 PM IST
    Geneva: The World Health Organization (WHO) and pharmaceutical company Eli Lilly and Co. are cautioning the public about fake versions of popular...
    USFDA Closes Inspection at Zydus Ankleshwar Unit-2 With Three Observations

    Cipla Goa facility gets 6 USFDA observations

    Ruchika Sharma22 Jun 2024 3:31 PM IST
    Mumbai: Pharma major, Cipla, has received six inspectional observations in Form 483 from the US Food and Drug Administration (USFDA) after...
    Johnson and Johnson Agrees to Cut US Drug Prices in Deal with Trump Administration to Avoid Tariffs

    JnJ seeks USFDA approval for Tremfya for moderately to severely active Crohn's disease

    Ruchika Sharma22 Jun 2024 2:21 PM IST
    Spring House: Johnson & Johnson has announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug...
    Sanofi India appoints Haresh Vala as Company Secretary, Compliance Officer

    Sanofi names Audrey Duval Derveloy as Executive Vice President, Global Head of Corporate Affairs

    Ruchika Sharma22 Jun 2024 12:47 PM IST
    Paris: Sanofi has announced the appointment of Audrey Duval Derveloy, a seasoned healthcare industry leader and Sanofi France's President as...
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