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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

    Caplin Steriles Secures USFDA Approval for Generic Methylprednisolone Injection

    Pfizer gets USFDA nod for Braftovi plus Mektovi for BRAF V600E-Mutant Metastatic Non-Small Cell Lung Cancer

    Ruchika Sharma14 Oct 2023 10:30 AM IST
    New York: Pfizer Inc. has announced that the U.S. Food and Drug Administration (FDA) has approved BRAFTOVI (encorafenib) + MEKTOVI (binimetinib)...
    India seeks corrective action from cough syrup firm Marion Biotech linked to Uzbek deaths

    India seeks corrective action from cough syrup firm Marion Biotech linked to Uzbek deaths

    Ruchika Sharma13 Oct 2023 3:57 PM IST
    "The firm will not carry out any medicine manufacturing work until the final decision of the appellate authority,"Gupta said.
    CDSCO Panel Denies Trial Waiver for Atropine, Asks Sun Pharma to Conduct Phase III Study

    Sun Pharma Cequa Phase 4 data shows sustained improvement in Dry Eye Disease signs, symptoms in patients switched from Restasis

    Ruchika Sharma13 Oct 2023 2:29 PM IST
    Mumbai: Sun Pharmaceutical Industries Limited has announced the presentation of Phase 4 data showing that CEQUA (cyclosporine ophthalmic solution)...
    Lupin secures SBTi validation for emission reduction targets

    Lupin gets tentative USFDA nod for generic equivalent of Xywav Oral Solution

    Ruchika Sharma13 Oct 2023 12:38 PM IST
    Lupin is exclusive first-to-file and may be eligible to receive a 180-day exclusivity period at product launch.
    Natco Pharma gets 7 USFDA observations for Kothur Pharma Division

    Panacea Biotec Pharma Baddi facility gets 9 USFDA observations

    Ruchika Sharma13 Oct 2023 11:30 AM IST
    Punjab: Panacea Biotec Limited has announced that the Company’s material wholly-owned subsidiary, Panacea Biotec Pharma Limited...
    Dr Reddys Labs inks pact with Henlius for commercialization of multiple myeloma injection HLX15 in US, Europe

    USFDA issues 9 observations for Dr Reddy's Labs Hyderabad facility

    Ruchika Sharma13 Oct 2023 10:30 AM IST
    Hyderabad: Pharma major, Dr Reddy's Labs, has announced that the United States Food & Drug Administration (USFDA) has concluded a product...
    Cipla arm New York facility gets EIR from USFDA

    Cipla arm New York facility gets EIR from USFDA

    Ruchika Sharma12 Oct 2023 3:30 PM IST
    Mumbai: Cipla has announced that the New York manufacturing facility of InvaGen Pharmaceuticals Inc., a wholly-owned subsidiary of the Company,...
    Goa Invokes ESMA, Bans Pharma Strikes for 6 Months

    No strike allowed in Goa pharma units, Govt extends ESMA by 6 months

    Ruchika Sharma12 Oct 2023 2:36 PM IST
    Panaji: With an aim of ensuring the uninterrupted production and supply of pharmaceuticals, the Goa government has decided to extend the Essential...
    Aster India unit draws suitors valuing business at USD 1.5 billion: Bloomberg

    Aster India unit draws suitors valuing business at USD 1.5 billion: Bloomberg

    Ruchika Sharma12 Oct 2023 1:30 PM IST
    New Delhi: Private equity firm BPEA EQT and Ontario Teachers’ Pension Plan Board are among firms considering a deal to acquire Aster DM Healthcare...
    Bristol Myers Squibb Breyanzi approved by USFDA for adults with Marginal Zone Lymphoma

    Bristol Myers Squibb Sotyktu long term data demonstrate durable efficacy, consistent safety for up to 3 years in moderate-to-severe Plaque Psoriasis

    Ruchika Sharma12 Oct 2023 12:50 PM IST
    Princeton: Bristol Myers Squibb has announced new three-year results from the POETYK PSO long-term extension (LTE) trial of Sotyktu...
    USFDA finds no misconduct at trial sites for Pfizer Lyme disease vaccine

    USFDA finds no misconduct at trial sites for Pfizer Lyme disease vaccine

    Ruchika Sharma12 Oct 2023 11:33 AM IST
    The Boston-based company denied allegations of breach of clinical trial guidelines, and said the USFDA's inspection did not result in any Form 483...
    India allows cough syrup firm linked to Uzbek deaths to re-open factory

    India allows cough syrup firm linked to Uzbek deaths to re-open factory

    Ruchika Sharma11 Oct 2023 5:30 PM IST
    New Delhi: India's northern state of Uttar Pradesh has permitted the resumption of most production at a factory owned by Marion Biotech, which...
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