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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

    Serum Institute seeks DCGI approval for phase 3 trial of Covovax as booster dose

    Serum Institute seeks DCGI approval for phase 3 trial of Covovax as booster dose

    MD Bureau28 Feb 2022 12:35 PM IST
    Covovax is approved by the European Medicines Agency for conditional marketing authorisation and also granted emergency use listing by WHO.
    Boehringer Ingelheim gets USFDA Breakthrough Therapy Designation for BI 1015550

    Boehringer Ingelheim gets USFDA Breakthrough Therapy Designation for BI 1015550

    MD Bureau28 Feb 2022 11:00 AM IST
    Germany: Boehringer Ingelheim has announced that the U.S. Food and Drug Administration (USFDA) has granted Breakthrough Therapy Designation to its...
    Moderna says COVID entering endemic phase, but annual vaccines will be needed

    Moderna says COVID entering endemic phase, but annual vaccines will be needed

    MD Bureau28 Feb 2022 10:00 AM IST
    Burton warned people will still get sick and die from Covid even when the virus becomes endemic.
    Bharat Biotech to come up with TB vaccine

    Bharat Biotech to come up with TB vaccine

    MD Bureau27 Feb 2022 11:30 AM IST
    Hyderabad: COVID-19 vaccine Covaxin maker Bharat Biotech International Limited is in the process of bringing out a vaccine against tuberculosis and...
    GSK Nucala application for COPD accepted for review in China

    GSK, Medicago get Health Canada nod for COVIFENZ

    MD Bureau27 Feb 2022 11:00 AM IST
    New Delhi: Medicago, a biopharmaceutical company headquartered in Quebec City, and GlaxoSmithKline (GSK) have recently announced that Health Canada...
    Pfizer supplemental application for ABRILADA interchangeability accepted by USFDA for review

    Pfizer supplemental application for ABRILADA interchangeability accepted by USFDA for review

    MD Bureau27 Feb 2022 10:30 AM IST
    New Delhi: Pfizer Inc. has announced that the U.S. Food and Drug Administration (USFDA) has accepted for review the Prior Approval Supplement (PAS) to...
    Moderna, Thermo Fisher Scientific expands collaboration for mRNA medicines

    Moderna, Thermo Fisher Scientific expands collaboration for mRNA medicines

    MD Bureau27 Feb 2022 10:00 AM IST
    New Delhi: Moderna, Inc. and Thermo Fisher Scientific Inc. have announced a 15-year strategic collaboration agreement to enable dedicated...
    USD 774 billion revenue opportunity for India from healthcare sector by 2030, suggests report

    USD 774 billion revenue opportunity for India from healthcare sector by 2030, suggests report

    MD Bureau27 Feb 2022 9:30 AM IST
    According to Bhatia, the top 10 ideas in the research can lead annual investment growth from USD 52 to USD 179 billion between 2020 and 2030 and grow...
    Online newsportal ordered to remove 14 articles on Bharat Biotech in Rs 100 crore defamation case

    Online newsportal ordered to remove 14 articles on Bharat Biotech in Rs 100 crore defamation case

    MD Bureau26 Feb 2022 4:21 PM IST
    Telangana: The Telangana Court ordered the Delhi-based news portal The Wire to take down 14 articles from their portal which they published on...
    Coronavirus vaccine sales push Moderna to USD 12 billion profit in 2021

    Coronavirus vaccine sales push Moderna to USD 12 billion profit in 2021

    MD Bureau26 Feb 2022 3:47 PM IST
    Washington: Moderna's COVID-19 vaccine brought in nearly USD 7 billion in the final quarter of 2021, and the drugmaker says it has signed purchase...
    Bulk drugs PLI Scheme: Minister interacts with Pharma companies

    Bulk drugs PLI Scheme: Minister interacts with Pharma companies

    MD Bureau26 Feb 2022 2:42 PM IST
    Total 49 projects approved for 33 critical APIs with a committed investment of Rs 3,685 crore.
    Eli Lilly, Boehringer Ingelheim gets USFDA nod for Jardiance to treat heart failure regardless of ejection fraction

    Eli Lilly, Boehringer Ingelheim gets USFDA nod for Jardiance to treat heart failure regardless of ejection fraction

    MD Bureau26 Feb 2022 11:00 AM IST
    Indianapolis: Eli Lilly and Company and Boehringer Ingelheim have recently announced that the U.S. Food and Drug Administration (USFDA) has...
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