Alembic Pharma gets US FDA approval for generic Levitra tablets
Alembic Pharmaceuticals Limited has received final approval from the US Food & Drug Administration (FDA) for its abbreviated new drug application (ANDA) vardenafil hydrochloride tablets, 2.5 mg (base), 5 mg (base), 10 mg (base), and 20 mg (base)
Biotechnology | 06/08/2020 | By Darshana | 480
FDA Revises Draft Guidance on Animal Drugs Intended for Minor Uses and Minor Species
The FDA encourages the development of safe and effective products to improve the health and well-being of all animals, including those for which there are limited options available because of the relatively small market they represent
Biotechnology | 20/07/2020 | By Darshana | 466
NRDC invites proposals for COVID-19 technologies for scaling up and validation
The National Research Development Corporation (NRDC), under the Department of Science and Technology (DST), has invited proposals from the innovators under its Department of Scientific and Industrial Research (DSIR) grants-in-aid promotional programme for development of technologies for commercialization (PDTC) for up-scaling the COVID-19
Biotechnology | 17/07/2020 | By Darshana | 306
GSK collaborates with Medicago to develop novel adjuvanted COVID-19 candidate vaccine
GSK and Medicago, a biopharmaceutical company, announced a collaboration to develop and evaluate a COVID-19 candidate vaccine combining Medicago's recombinant Coronavirus Virus-Like Particles (CoVLP) with GSK's pandemic adjuvant system
Biotechnology | 09/07/2020 | By Darshana | 399
Thermo Fisher Scientific launches serology testing kit for infectious diseases
Thermo Fisher Scientific, the world leader in serving science, today announced the availability of the Thermo Scientific MAS Omni Infectious Disease quality control sets for monitoring serological assays for analytes such as HIV 1&2, Hepatitis B & C virus, Syphilis and HTLV I/II
Biotechnology | 07/07/2020 | By Darshana | 441
The European Commission has granted Orphan Medicinal Product Designation in the EU for MIV-818
Medivir today announced that the European Commission, in accordance with the opinion from the European Medicines Agency (EMA), has granted orphan medicinal product designation in the EU for MIV-818 for the treatment of patients with hepatocellular carcinoma (HCC), the most common type of primary liver cancer
Biotechnology | 05/07/2020 | By Darshana | 372
NPPA fixes retail prices of 14 formulations under DPCO 2013
NPPA has fixed retail prices of 14 formulations under Drugs Prices Control Order (DPCO)- 2013 relating to 76th Authority meeting dated June 22, 2020.
Biotechnology | 03/07/2020 | By Darshana | 641
Selumetinib granted orphan drug designation in Japan for neurofibromatosis type 1
AstraZeneca today announced that selumetinib has been granted orphan drug designation (ODD) in Japan for the treatment of neurofibromatosis type 1 (NF1), a rare and debilitating genetic disease
Biotechnology | 01/07/2020 | By Darshana | 349
'COVAXIN': India's first Covid vaccine gets DGCI's approval for clinical trials
Bharat Biotech, has successfully developed Covaxin, India's 1st vaccine candidate for COVID-19, in collaboration with the Indian Council of Medical Research (ICMR) and the National Institute of Virology (NIV). The SARS-CoV-2 strain was isolated in NIV, Pune and transferred to Bharat Biotech
Biotechnology | 30/06/2020 | By Darshana | 285
Hetero Healthcare set to supply 20,000 vials of generic remdesivir across country
Following the approval of "Covifor", the generic of remdesivir by DCGI, Hetero Healthcare Limited, a group company of Hetero is set to deliver the first set of 20,000 vials in two equal lots of 10,000 each
Biotechnology | 25/06/2020 | By Darshana | 316
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