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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

    Boehringer Ingelheim, LEO Pharma collaborate

    Boehringer Ingelheim, Cue Biopharma partner to develop next generation treatment for autoimmune, inflammatory diseases

    Ruchika Sharma16 April 2025 10:30 AM IST
    Boston: Boehringer Ingelheim and Cue Biopharma, Inc. have announced a strategic research collaboration and license agreement to develop and...
    Bristol Myers Squibb bags European Commission approval for Opdivo combo in lung cancer treatment

    Bristol Myers Squibb heart disease drug fails to meet main goals in late-stage study

    Ruchika Sharma16 April 2025 9:30 AM IST
    Princeton: Bristol Myers Squibb has announced the Phase 3 ODYSSEY-HCM trial evaluating Camzyos (mavacamten) for the treatment of adult...
    Bristol Myers Squibb, Bain Capital form new biopharmaceutical company - NewCo

    Mankind Pharma to constitute committee to evaluate ways to integrate BSV

    Ruchika Sharma15 April 2025 5:17 PM IST
    New Delhi: Mankind Pharma has announced that the Board of Directors of the Company at its meeting has inter-alia, considered and approved the...
    Biocon appoints Ekta Agarwal as Interim Company Secretary, Compliance Officer

    Biocon Biologics secures market entry date for ophthalmology drug Yesafili in US

    Ruchika Sharma15 April 2025 4:18 PM IST
    Additionally, Biocon Biologics secured a settlement agreement in Canada with Bayer and Regeneron Pharma for launch of YESAFILI no later than July 1,...
    AstraZeneca Pharma India surrenders marketing authorisation for specific indication of Olaparib

    AstraZeneca Pharma India surrenders marketing authorisation for specific indication of Olaparib

    Ruchika Sharma15 April 2025 3:46 PM IST
    Bangalore: AstraZeneca Pharma India Limited has surrendered its marketing authorisation for Olaparib film-coated tablets 100mg and 150mg...
    India Cuts API Imports, Disburses Rs 1,008 Cr Under PLI Schemes, Parliament Told

    Delhi: Counterfeit Thrombophob Ointments worth over Rs 2.5 Lakh seized following Zydus Healthcare complaint

    Ruchika Sharma15 April 2025 12:49 PM IST
    New Delhi: Acting on a complaint filed by pharmaceutical major Zydus Healthcare Limited, the Drugs Control Department of the Delhi government has...
    JnJ receives USFDA Approval for updated Varipulse Platform Irrigation Rate

    Johnson & Johnson MedTech completes first cases with OTTAVA Robotic Surgical System

    Ruchika Sharma15 April 2025 11:45 AM IST
    Upon completion of the study, the company plans to submit the OTTAVA system for De Novo authorization in the United States.
    Whos going to pay price to bring back manufacturing in US, asks Biocon MD

    "Who's going to pay price to bring back manufacturing in US", asks Biocon MD

    Ruchika Sharma15 April 2025 10:30 AM IST
    New Delhi: Siddharth Mittal, the CEO and Managing Director of Biocon Limited, raised a critical question on Friday, asking who would bear...
    Pfizer discontinues development of danuglipron for chronic weight management

    Pfizer discontinues development of danuglipron for chronic weight management

    Ruchika Sharma14 April 2025 5:41 PM IST
    New York: Pfizer Inc. has announced the company has discontinued the development of danuglipron (PF-06882961), an oral glucagon-like...
    Multi-drug resistant infections medicine Zaynich to get USFDA approval next year: Wockhardt Chairman

    Multi-drug resistant infections medicine 'Zaynich' to get USFDA approval next year: Wockhardt Chairman

    Ruchika Sharma14 April 2025 3:49 PM IST
    Dubai: Zaynich, a multi-drug resistant infections medicine, is set to receive the US Food and Drug Administration (USFDA) approval in 2026,...
    Sandoz to acquire Just-Evotec Biologics EU SAS in-house development, manufacturing capabilities in France for USD 300 million

    Arthritis drug: Sandoz files US antitrust litigation against Amgen

    Ruchika Sharma14 April 2025 2:30 PM IST
    Sandoz is seeking an injunction to prevent Amgen from using certain patent rights to block biosimilar competition and allow Sandoz to launch Erelzi.
    Sun Pharma, Zydus and Glenmark recall various products in US over manufacturing issues

    Sun Pharma, Zydus and Glenmark recall various products in US over manufacturing issues

    Ruchika Sharma14 April 2025 1:30 PM IST
    Sun Pharma, Zydus, and Glenmark are recalling various products in the US market due to manufacturing-related concerns, the US health regulator...
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