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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

    Mylan Pharma gets USFDA nod for Breyna for Generic Version of Symbicort

    Mylan Pharma gets USFDA nod for Breyna for Generic Version of Symbicort

    MD Bureau17 March 2022 3:29 PM IST
    Viatris Inc. and Kindeva Drug Delivery L.P. today announced that Mylan Pharmaceuticals Inc. has received approval from the U.S. Food and Drug...
    GSK Nucala application for COPD accepted for review in China

    GSK announces appointment of six directors to Designate Haleon Board

    MD Bureau17 March 2022 12:43 PM IST
    GlaxoSmithKline plc today announced the appointment of six directors to the designate Board of Haleon, the new independent company to be formed...
    Sanofi announces €300 million collaboration with Blackstone Life Sciences

    Sanofi announces €300 million collaboration with Blackstone Life Sciences

    MD Bureau17 March 2022 10:43 AM IST
    For the Sarclisa subcutaneous formulation delivery, Sanofi has partnered with drug delivery technology innovator company Enable Injections, Inc. to...
    Niramai gets USFDA nod for  medical device SMILE-100 System

    Niramai gets USFDA nod for medical device SMILE-100 System

    MD Bureau16 March 2022 5:19 PM IST
    Niramai Health Analytix, the deep-tech Bangalore-based healthcare company offering a novel radiation-free, non-touch, accurate, breast cancer...
    Pfizer, Bayer to maintain essential drug supply to Russia

    Pfizer, Bayer to maintain essential drug supply to Russia

    MD Bureau16 March 2022 3:44 PM IST
    Pfizer Inc and Bayer said on Monday they would maintain humanitarian supply of medicines to Russia, but would pull back from other non-essential...
    Alembic Pharma receives USFDA Tentative Approval for Macitentan

    Alembic Pharma receives USFDA Tentative Approval for Macitentan

    MD Bureau16 March 2022 3:42 PM IST
    The tentatively approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Opsumit Tablets, 10 mg, of Actelion...
    Zydus Lifesciences gets USFDA nod for  Colestipol Hydrochloride Tablets

    Zydus Lifesciences gets USFDA nod for Colestipol Hydrochloride Tablets

    MD Bureau16 March 2022 3:41 PM IST
    Colestipol hydrochloride tablets are indicated as adjunctive therapy to diet for the reduction of elevated serum total and LDL-C in patients with...
    BioMed X Institute announces new research project in collaboration with Merck

    BioMed X Institute announces new research project in collaboration with Merck

    MD Bureau15 March 2022 3:43 PM IST
    A German independent research institute, BioMed X, announces today the start of its new research project 'Regulatory T Cell Dysfunction in...
    No USFDA approval for  AstraZenecas treatment for chronic nasal condition

    No USFDA approval for AstraZeneca's treatment for chronic nasal condition

    MD Bureau15 March 2022 3:02 PM IST
    The London-listed drugmaker said the U.S. Food and Drug Administration (FDA) had issued a complete response letter following AstraZeneca's application...
    Novavaxs COVID vaccine rollout in EU off to a slow start -data

    Novavax's COVID vaccine rollout in EU off to a slow start -data

    MD Bureau15 March 2022 2:42 PM IST
    The Novavax vaccine, the latest to receive the EU regulators' approval under the trade name of Nuvaxovid, was expected to persuade some sceptics...
    PLI scheme for bulk drugs, DoP extends deadline

    PLI scheme for bulk drugs, DoP extends deadline

    MD Bureau15 March 2022 2:41 PM IST
    Department is implementing three PLI schemes viz PLI scheme for Bulk Drugs (Rs.6,940 Cr), PLI scheme for Medical Devices (Rs.3,420 Cr) and PLI scheme...
    Gan & Lee Pharmaceuticals Begins First-In-Human Trial of  GZR18

    Gan & Lee Pharmaceuticals Begins First-In-Human Trial of GZR18

    MD Bureau15 March 2022 9:00 AM IST
    The primary objective of this Phase 1 study is to investigate the safety and tolerability of GZR18 in healthy volunteers. In addition, the secondary...
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