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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

    Himachal Pradesh CM inaugurates Bulk Drug Park in Una

    Himachal Pradesh CM inaugurates Bulk Drug Park in Una

    Ruchika Sharma21 Jun 2024 12:30 PM IST
    Himachal Pradesh: Chief Minister Thakur Sukhvinder Singh Sukhu has inaugurated the commencement of the Bulk Drug Park constructed at Panjuvana in...
    Child Given Wrong Injection at Government Hospital

    Zydus group refutes media report claiming suspension of Biotax sales in Nepal, says will sell antibiotic with 10ml sterile water

    Ruchika Sharma21 Jun 2024 11:30 AM IST
    New Delhi: Zydus group announced its decision to make available its antibiotic injection Biotax 1g with 10ml sterile water in Nepal, responding...
    AstraZeneca announces Rs 176 crore investments in India to expand Chennai GITC

    AstraZeneca Truqap, Faslodex combo approved in EU for advanced ER-positive breast cancer

    Ruchika Sharma21 Jun 2024 10:00 AM IST
    Cambridge: AstraZeneca has announced that Truqap (capivasertib) in combination with Faslodex (fulvestrant) has been approved in the...
    KKR divests 5.8 percent stake in JB Chemicals & Pharma for Rs 1460 crore

    Gland Pharma promoter Fosun divests 6 percent stake for Rs 1,754 crore

    Ruchika Sharma20 Jun 2024 2:48 PM IST
    Fosun Pharma, a promoter in Gland Pharma, has executed a significant divestment by selling a 6 per cent stake for Rs 1,754 crore through an open...
    Meril Life Sciences announces LANCET publication for landmark RCT of MYVAL THV series, researched and developed by India

    Meril Life Sciences announces LANCET publication for landmark RCT of MYVAL THV series, researched and developed by India

    Ruchika Sharma20 Jun 2024 1:30 PM IST
    New Delhi: Meril Life Sciences has announced the publication of the LANDMARK trial study titled "Comparison of Early Outcomes of Newer-Generation...
    Sun Pharma Halol facility gets OAI status from USFDA

    USFDA issues warning letter to Sun Pharma Dadra facility

    Ruchika Sharma20 Jun 2024 12:34 PM IST
    Mumbai: Sun Pharmaceutical Industries Limited has received a Warning Letter from the US Food and Drug Administration (USFDA) for its Dadra...
    Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

    JnJ submits application to USFDA for Subcutaneous amivantamab for patients with EGFR-mutated non-small cell lung cancer

    Ruchika Sharma19 Jun 2024 3:56 PM IST
    Raratin: Johnson & Johnson has announced the submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration...
    Cipla Bommasandra facility gets VAI classification from USFDA

    Cipla EU to infuse additional EUR 3 million in Ethris

    Ruchika Sharma19 Jun 2024 2:53 PM IST
    Mumbai: Cipla Limited has announced that its wholly-owned subsidiary in United Kingdom, Cipla (EU) Limited will invest an additional EUR 3...
    Lalitpur Pharma Park

    USFDA nod to Alembic Pharma stroke and blood clots drug Dabigatran Etexilate

    Ruchika Sharma19 Jun 2024 12:12 PM IST
    Vadodara: Alembic Pharmaceuticals Limited has announced that it has received final approval from the US Food & Drug Administration (USFDA)...
    AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

    USFDA issues 15 observations for Jubilant HollisterStier General Partnership Montreal facility

    Ruchika Sharma19 Jun 2024 11:15 AM IST
    Noida: Jubilant Pharmova Limited has announced that the United States Food and Drug Administration (USFDA) has concluded the audit of the...
    USFDA approves Takeda Gammagard liquid ERC for primary immunodeficiency

    Takeda announces Phase 3 topline results for Soticlestat in patients with Dravet Syndrome, Lennox-Gastaut Syndrome

    Ruchika Sharma18 Jun 2024 4:14 PM IST
    Osaka: Takeda has announced topline data from its SKYLINE and SKYWAY studies. SKYLINE (TAK-935-3001) was a multicenter, randomized, double-blind...
    Emcure Pharma arm Gennova advances development of Nipah virus vaccine

    Merck Capvaxive gets USFDA nod for prevention of Invasive Pneumococcal Disease, Pneumococcal Pneumonia in adults

    Ruchika Sharma18 Jun 2024 2:04 PM IST
    Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the U.S. Food and Drug Administration (FDA) has approved...
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