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MD Bureau
MD Bureau

    Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in.

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    Articles By : MD Bureau

    Pfizer recalls blood pressure drug Accuretic due to potential carcinogen

    Pfizer recalls blood pressure drug Accuretic due to potential carcinogen

    MD Bureau22 March 2022 5:26 PM IST
    Pfizer said it has not received any reports of adverse events related to the drug till date.
    Hester Biosciences Limited ventures into Pet Care Industry

    Hester Biosciences Limited ventures into Pet Care Industry

    MD Bureau22 March 2022 5:25 PM IST
    Hester’s comprehensive knowledge of animal biology, cutting-edge R&D capabilities, and four-decade-long experience in animal healthcare gives them an...
    Sun Pharma

    Sun Pharma to acquire Daiichi's 11.28 percent stake in Zenotech

    MD Bureau22 March 2022 4:34 PM IST
    After the acquisition, Sun Pharma's stake in Zenotech will increase from 57.56 percent to 68.84 percent.
    Kilitch Drugs starts Rs. 100 crore New Facility Expansion Plan

    Kilitch Drugs starts Rs. 100 crore New Facility Expansion Plan

    MD Bureau22 March 2022 4:28 PM IST
    Mukund Mehta, Chairman & Managing Director of Kilitch Drugs, said, "We are on a growth trajectory and demand for our products is increasing. This...
    Zydus gets USFDA Prior Approval Supplement (PAS) approval for Mycophenolate Mofetil for Injection USP

    Zydus gets USFDA Prior Approval Supplement (PAS) approval for Mycophenolate Mofetil for Injection USP

    MD Bureau21 March 2022 4:41 PM IST
    The injection will be manufactured at the groups injectables manufacturing facility at Jarod near Vadodara in Gujarat.
    Moderna Announces New Supply Agreement with Switzerland for Additional Seven Million  Doses of COVID-19 Booster Vaccine

    Moderna Announces New Supply Agreement with Switzerland for Additional Seven Million Doses of COVID-19 Booster Vaccine

    MD Bureau21 March 2022 4:34 PM IST
    These doses are in addition to the seven million doses of Moderna's booster vaccine that are scheduled for supply to Switzerland in the second half of...
    Glenmark Pharmaceuticals receives ANDA approval for Lacosamide Tablets

    Glenmark Pharmaceuticals receives ANDA approval for Lacosamide Tablets

    MD Bureau21 March 2022 3:48 PM IST
    According to IQVIA sales data for the 12 month period ending January 2022, the Vimpat Tablets, 50 mg, 100 mg, 150 mg and 200 mg market3 achieved...
    CDSCO nod to Wockhardt 3-day treatment for Community-Acquired Bacterial Pneumonia

    Wockhardt , Serum Life Sciences collaborate for manufacturing multiple vaccines

    MD Bureau21 March 2022 12:54 PM IST
    This collaboration between a subsidiary of Wockhardt and Serum Life Sciences UK will help create considerable number of employment opportunities...
    Granules India Receives Licences from MPP to Market generic of Pfizers Paxlovid

    Granules India Receives Licences from MPP to Market generic of Pfizers Paxlovid

    MD Bureau21 March 2022 11:46 AM IST
    The product will be made at Granules manufacturing facilities in India that are approved by global regulatory agencies including USFDA. The license...
    Oppilotech and Evariste Technologies Announce Partnership to Develop First-in-Class Antibacterial Programme

    Oppilotech and Evariste Technologies Announce Partnership to Develop First-in-Class Antibacterial Programme

    MD Bureau20 March 2022 4:45 PM IST
    Oppilotech Ltd, a biotech specialising in systems biology and machine learning platforms to build unique predictive computational models of cells,...
    Bristol Myers  gets USFDA approval  for First LAG-3-Blocking Antibody Combination, Opduala

    Bristol Myers gets USFDA approval for First LAG-3-Blocking Antibody Combination, Opduala

    MD Bureau20 March 2022 2:30 PM IST
    The trial met its primary endpoint, progression-free survival, and Opdualag more than doubled the median PFS when compared to nivolumab monotherapy,...
    Moderna submits amendment to USFDA for its COVID-19 vaccine booster dose

    Moderna submits amendment to USFDA for its COVID-19 vaccine booster dose

    MD Bureau20 March 2022 2:15 PM IST
    The U.S. FDA approved the Biologics License Application (BLA) for SPIKEVAX (COVID-19 Vaccine, mRNA) to prevent COVID-19 in individuals 18 years of age...
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