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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 Canada recalls BP drug  on potential cancer-causing impurity

    Pfizer Canada recalls BP drug on potential cancer-causing impurity

    MD Bureau7 March 2022 11:49 AM IST
    Patients can continue to take their medication as prescribed and do not need to return the drug to their pharmacy, the agency said, but asked patients...
    PG Medical Admissions Under Management Quota: KNRUHS issues notice on web options, Details

    PG Medical Admissions Under Management Quota: KNRUHS issues notice on web options, Details

    MD Bureau7 March 2022 9:30 AM IST
    Telangana : The KNRUHS has recently issues a Notification for Exercising web options for second phase counselling of PG Medical Degree/Diploma...
    PFIZER Clostridium difficile Vaccine did not meet primary endpoints: PHASE 3 CLOVER Trial

    PFIZER Clostridium difficile Vaccine did not meet primary endpoints: PHASE 3 CLOVER Trial

    MD Bureau6 March 2022 1:29 PM IST
    New York: Pfizer Inc. announced results from the CLOVER trial (CLOstridium difficile Vaccine Efficacy TRial), a pivotal Phase 3 study evaluating its...
    Pfizers bacteria prevention vaccine fails at main stage

    Pfizer's bacteria prevention vaccine fails at main stage

    MD Bureau5 March 2022 1:27 PM IST
    The infection is associated with diarrhea that may progress to a severe and debilitating illness and even result in death.
    CDSCO nod to Wockhardt 3-day treatment for Community-Acquired Bacterial Pneumonia

    Wockhardt sets issue price at Rs 225 per share for Rs 748-cr rights issue

    MD Bureau5 March 2022 1:21 PM IST
    The issue price has been fixed at Rs 225 per fully paid-up equity share, including a premium of Rs 220 per share.
    USFDA issues 3 minor observations to Granules India arm in pre-approval inspection

    USFDA issues 3 minor observations to Granules India arm in pre-approval inspection

    MD Bureau4 March 2022 12:38 PM IST
    Commenting on the audit, GPI Executive Director Priyanka Chigurupati said, "We are glad to have completed yet another audit with minor observations...
    WHO recommends Molnupiravir for high risk patients

    WHO recommends Molnupiravir for high risk patients

    MD Bureau4 March 2022 12:09 PM IST
    The expert panel conditionally recommended the pill, molnupiravir, for patients with the non-severe disease who are at high risk of hospitalization.
    Lupins Efinaconazole Topical Solution gets USFDA nod

    Lupin's Efinaconazole Topical Solution gets USFDA nod

    MD Bureau4 March 2022 12:09 PM IST
    Lupin today announced that it has received approval from the USFDA for its ANDA, Efinaconazole Topical Solution, 10%to market a generic equivalent of...
    Takeda appoints Serina Fischer as General Manager for India operations

    Takeda appoints Serina Fischer as General Manager for India operations

    MD Bureau3 March 2022 5:23 PM IST
    In her new role, Serina will lead the company's business in India, ensuring patient access to the company's highly innovative medicines, the drug firm...
    Study: Pfizer-BioNTech Covid vaccine less effective in kids

    Study: Pfizer-BioNTech Covid vaccine less effective in kids

    MD Bureau3 March 2022 2:07 PM IST
    The study, led by The New York State Department of Health, found that during the Omicron era, the effectiveness of the Pfizer-BioNTech Covid vaccine...
    Lupin gets USFDA nod for  Sevelamer Hydrochloride Tablets

    Lupin gets USFDA nod for Sevelamer Hydrochloride Tablets

    MD Bureau3 March 2022 2:05 PM IST
    Sevelamer Hydrochloride Tablets, 800 mg is a generic equivalent of Renagel® Tablets, 800 mg of Genzyme Corporation.
    GC Pharma gets CRL from USFDA for ALYGLO

    GC Pharma gets CRL from USFDA for ALYGLO

    MD Bureau2 March 2022 4:01 PM IST
    The FDA issues a complete response letter to indicate that the review cycle for an application is complete but the application cannot be approved in...
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