WHO urges âimmediateâ action on falsified medicines
The WHO called on stakeholders in various nations to take âimmediate and coordinated actionâ to shield children from using contaminated cough syrups following.
Bharti Rana Jayshankar – Founder
She brings in more than 30 years of experience in content building, architecture, writing, editing and storytelling. Ms Jayshankar has worked in the Economic Times daily, IBT Times, Investopedia and more than a dozen content firms as a content strategist and planner.
Jay Shankar – Co-founder
He has almost three decades of experience in journalism. He has worked with national dailies such as ET, Indian Express, The Pioneer, The Hindu, Agence France Presse and Bloomberg.
The WHO called on stakeholders in various nations to take âimmediate and coordinated actionâ to shield children from using contaminated cough syrups following.
Merck says its diabetes drugs got contaminated during storage and manufacturings and it will improve the same to prevent it in future
More than 131 million people in the Latin American and Caribbean population are not able to afford a healthy diet, due to high.
Johnson & Johnson stopped the phase III trial of its global HIV vaccine trial after it found that the regimen was ineffective in.
India is bolstering its regulatory bodies to global standards to become a world leader in drug discovery and innovative medical devices, a minister.
Glenmark Pharmaceuticals, an Indian multinational firm, has introduced its heart failure drug in the country, according to a company statement.
Pharma major Lupin has received a âtentative approvalâ, from the United States Food and Drug Administration (FDA), to market medicines used to treat.
The USFDA has granted Zydus Lifesciences Limited âtentative approvalâ to market Levomilnacipran extended-release capsules in 20 mg, 40 mg, 80 mg, and 120.
The Indian pharmaceutical industry is expected to witness âdecent growthâ during the three-month period through 31 March 2023, mainly led by continued traction.
Eiasi Co., a Japanese pharmaceutical company, has submitted a marketing authorization application for a drug, lacanemab, to treat Alzheimer's disease.
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