Siemens Healthineers bags first US FDA EUA for semi-quantitative SARS-CoV-2 IgG antibody test
Siemens Healthineers has received FDA Emergency Use Authorization (EUA) for the SARS-CoV-2 IgG (COV2G) antibody test. Like all…
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US FDA
Unichem Laboratories gets USFDA nod to market muscle spasm tablets
The tablets will be commercialised from the company's Goa plant
Drug firm Unichem Laboratories has received approval from the…
73 per cent doctors cite ‘antiviral agents’ as most effective therapy for treating COVID-19: Course5…
Global fight against COVID-19 has found powerful tools in form AI, ML, big data, IoT technologies that are playing key role in…
Abbott receives FDA approval for its ICD, CRT-D devices
The devices bring new benefits to patients with heart rhythm disorders, including patient-preferred design without compromising…
Drug firms in India recall products from US
While Lupin and Marksans Pharma are recalling diabetes drug, Aurobindo and Alembic are recalling psychiatric medication in the US…
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Transasia Bio-Medicals receives US FDA registration for in-vitro diagnostic instruments manufactured…
Transasia’s ‘Made in India’ products which are currently exported to over 100 countries will now also be available in the US
US FDA comes out with guidance for COVID-19 vaccine approval
More than 100 vaccines are being tested worldwide against the virus
The US Food and Drug Administration released…
Abbott finalises agreement with Tandem Diabetes Care
To develop, commercialise integrated diabetes solutions that combine Abbott's CGM technology with Tandem's innovative insulin…
Kiyou Jochugiku launches ‘Air Doctor’ in India
The portable product helps to prevent viruses, bacteria, fungus within one metre radius
Oncomine Precision Assay receives breakthrough device designation by FDA
The assay can be used to identify low-grade glioma patients with isocitrate dehydrogenase IDH1, IDH2 mutation