BELLUS Health Convenes Virtual KOL Meeting to Discuss the State of Chronic Cough Treatment
Bellus a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of chronic cough and other hypersensitization-related disorders, today announced that it will convene a virtual Key Opinion Leader (KOL) meeting to discuss the chronic cough landscape on Wednesday, May 27, 2020 at 9:00 a.m. EDT
Biotechnology | 15/05/2020 | By Darshana | 297
ICMR notifies NIMHANS as mentor institution for RT-PCR test protocol for COVID-19
The National Institute of Mental Health and Neuro Sciences (NIMHANS) has been notified by the Indian Council of Medical Research (ICMR) and the Medical Council of India (MCI) as the mentor institution for RT-PCR (Reverse transcription-polymerase chain reaction) test
Biotechnology | 10/05/2020 | By Darshana | 260
Hydroxychloroquine and Chloroquine Marketto more than Double in 2020 ? TechSci Research
Increase in prevalence of COVID-19 to drive demand for hydroxychloroquine and chloroquine across the globe
Biotechnology | 29/04/2020 | By Darshana | 164
Alembic Pharma gets US FDA approval for Lastacaft ophthalmic solution
Alembic Pharmaceuticals Limited has received tentative approval from the US Food & Drug Administration (FDA) for its abbreviated new drug application (ANDA) alcaftadine ophthalmic solution, 0.25%
Biotechnology | 21/04/2020 | By Darshana | 712
Oncolytics Biotech updates clinical development & operations activities during COVID-19 pandemic
Oncolytics Biotech Inc., currently developing pelareorep, an intravenously delivered immuno-oncolytic virus, provided an update on the potential impact of COVID-19 on the company's clinical and business operations
Biotechnology | 20/04/2020 | By Darshana | 268
FDA Encourages Recovered Patients to Donate Plasma for Development of Blood-Related Therapies
As part of the all-of-America approach to fighting the COVID-19 pandemic, the U.S. Food and Drug Administration has been working with partners across the U.S. government, academia and industry to expedite the development and availability of critical medical products to treat this novel virus
Biotechnology | 19/04/2020 | By Darshana | 251
Abbott announced that the US Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the fastest available molecular point-of-care test for the detection of novel coronavirus (COVID-19), delivering positive results in as little as five minutes and negative results in 13 minutes
Biotechnology | 30/03/2020 | By Darshana | 844
Mylab Ships First Batch of COVID 19 Test Kits To Government And Private Labs
First batch of Made in India Testing kit for Covid-19 to be shipped today, Government and private labs approved by ICMR to conduct tests. Mylab can ramp-up capacity from 20,000 to 50,000 kits a day if needed
Biotechnology | 27/03/2020 | By Darshana | 571
First Made in India COVID-19 tests kit by Mylab gets commercial approval from the government
Mylab is the first Indian company getting commercial COVID-19 PCR kit approved by CDSCO.Mylab COVID-19 test kits cost nearly one-fourth of the currently procured kits. Mylab uses advanced protocols which can reduces testing time by 65%
Biotechnology | 24/03/2020 | By Darshana | 1175
DST invites proposals for prevention and therapy of COVID-19
The Technology Development Board (TDB), a statutory body under Department of Science and Technology (DST) has invited proposal applications from Indian companies to address protection and home-based therapeutic respiratory intervention for coronavirus (COVID-19) patients.
Biotechnology | 24/03/2020 | By Darshana | 391
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