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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

    AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

    AstraZeneca Truqap plus Faslodex recommended for approval in EU by CHMP for advanced ER-positive breast cancer

    Written By Ruchika Sharma1 May 2024 11:30 AM IST
    Cambridge: AstraZeneca's Truqap (capivasertib) in combination with Faslodex (fulvestrant) has been recommended for approval in the...
    AstraZeneca admits very rare side effect of COVID vaccine in UK court

    AstraZeneca admits 'very rare' side effect of COVID vaccine in UK court

    Written By Ruchika Sharma30 April 2024 6:00 PM IST
    London: AstraZeneca (AZ), a pharmaceutical giant headquartered in the UK, has acknowledged that in "very rare cases," its coronavirus vaccine can...
    CDSCO Panel Accepts Glenmarks Apremilast Trial Report, Seeks 2-Year PSUR Data

    Glenmark Pharma gets USFDA nod for Acetaminophen and Ibuprofen Tablets

    Written By Ruchika Sharma30 April 2024 5:50 PM IST
    New Jersey: Glenmark Pharmaceuticals Ltd. has received final approval from the United States Food & Drug Administration (U.S. FDA)...
    Sanofis Sarclisa Gets EMA Nod for Subcutaneous On-Body Injector Version

    Diabetes drug: Sanofi unveils Soliqua in India

    Written By Ruchika Sharma30 April 2024 2:35 PM IST
    Soliqua is a once-daily injectable combination drug containing insulin glargine 100 Units/ml, which is a long-acting basal insulin and lixisenatide, a...
    Granules India arm gets USFDA nod for Gout flares drug Colchicine

    Granules India arm gets USFDA nod for Gout flares drug Colchicine

    Written By Ruchika Sharma30 April 2024 11:30 AM IST
    Colchicine Capsules are indicated for prophylaxis of gout flares in adults.
    Gland Pharma profit rises 12 percent to Rs 184 crore in Q2

    Gland Pharma bags USFDA nod for Cetrorelix Acetate for Injection

    Written By Ruchika Sharma29 April 2024 3:06 PM IST
    Cetrorelix Acetate for Injection is used to prevent premature LH surges in women undergoing controlled ovarian stimulation.
    Prior Intimation System Under NDCT Rules Wont Apply to Hormones, Cytotoxics, Beta-Lactams, Certain Biologics: CDSCO

    India becoming attractive for clinical trials: Pharma industry leaders

    Written By Ruchika Sharma29 April 2024 2:33 PM IST
    New Delhi: Experts from the pharmaceutical sector have noted that over the last decade, clinical trials in India have undergone significant...
    Johnson and Johnson Agrees to Cut US Drug Prices in Deal with Trump Administration to Avoid Tariffs

    JnJ gets positive CHMP opinion for Rybrevant, chemotherapy combo for first-line treatment of patients with advanced non-small cell lung cancer with activating EGFR exon 20 insertion mutations

    Written By Ruchika Sharma28 April 2024 12:30 PM IST
    Belgium: Janssen-Cilag International NV, a Johnson & Johnson company, has announced that the Committee for Medicinal Products for Human Use...
    Global Fund expands commitment to improve access to HIV drug

    USFDA approves Biktarvy label update with data for pregnant adults with HIV: Gilead Sciences

    Written By Ruchika Sharma28 April 2024 11:30 AM IST
    Foster City: Gilead Sciences, Inc. has announced the U.S. Food and Drug Administration (FDA) has approved an updated label with additional data...
    CDSCO Panel Clears Bristol Myers Yervoy for Two New Cancer Indications

    EMA Committee recommends nod for Bristol Myers Squibb Opdivo in combination with Cisplatin, Gemcitabine for Urothelial Carcinoma

    Written By Ruchika Sharma28 April 2024 11:30 AM IST
    Princeton: Bristol Myers Squibb has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines...
    Pfizer Secures Vyndamax Patent Till 2031

    USFDA nod to Pfizer Beqvez for adults with Hemophilia B

    Written By Ruchika Sharma27 April 2024 12:09 PM IST
    New York: Pfizer Inc. has announced that the U.S. Food and Drug Administration (FDA) has approved BEQVEZ (fidanacogene elaparvovec-dzkt) for the...
    Palamur Biosciences Faces USFDA Warning for Multiple GLP Compliance Failures

    Zydus Lifesciences bags USFDA nod for acne cream Tretinoin

    Written By Ruchika Sharma27 April 2024 11:39 AM IST
    Ahmedabad: Zydus Lifesciences Limited has announced that the Company has received final approval from the United States Food and Drug...
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