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EUROPEAN MEDICINES AGENCY
Wockhardt shares rocket 19% after FDA approval for antibiotic targeting drug-resistant infections. Check detailsWockhardt's shares surged 19% after the U.S. FDA approved ZAYNICH, a novel intravenous antibiotic for complicated urinary tract infections....- What to know about the outbreak of a rare kind of Ebola as cases outpace responseA rare Ebola outbreak is spreading rapidly in Congo and Uganda. The Bundibugyo virus has no approved treatments. Health workers face challe...
- Sensex surges over 800 points to cross 75,400; Nifty above 23,650 despite weak rupeeIn a recent turn of fortunes, Indian stock markets experienced a notable rise for the second consecutive day. On Thursday, both the Sensex ...
- Chinese medicines bring relief to India’s cancer patientsIndia’s cancer treatment landscape is seeing a shift as lower-cost immunotherapy drugs developed in China and marketed through Indian partn...
- Rare but ruthless: How Hantavirus strikes fast, and should you be concernedA rare hantavirus outbreak linked to a cruise ship has drawn global attention after multiple infections and three reported deaths prompted ...
- Soleno withdraws EU rare disease drug application ahead of Neurocrine takeoverSoleno Therapeutics has withdrawn its European drug application. This decision stems from its acquirer, Neurocrine Biosciences, prioritizin...
- EU forgoes 100 million J&J vaccine, likely to donate other dosesThe EU at the end of March let the term to order 100 million extra doses lapse, three European officials with direct knowledge of contracts...
- EU drug agency discounts any link between AstraZeneca covid vaccine and clotsThe head of the EMA, Emer Cooke said Thursday that the agency "cannot rule out definitively a link" between rare types of blood clots and t...
- EU reviews BioNTech request for 'extra dose' of virus shotIn an email to The Associated Press, the European Medicines Agency said that BioNTech, which developed its vaccine together with Pfizer, ha...
- Pfizer-BioNTech's Covid-19 vaccine: Path ahead in UKThe country's state-run National Health Service (NHS) will be charged with conducting the mass vaccination programme over the subsequent we...
- EU defends vaccine trials as UK gives first OKBritish ministers claimed Brexit has allowed them to adopt the Pfizer-BioNTech vaccine ahead of their neighbours, who are still awaiting a ...
- SeQuent Scientific launches veterinary medicine in 19 European countriesThe product had recently received approval from European Medicines Agency (EMA) through its Spanish subsidiary Laboratorios Karizoo, S A, t...
- Remdesivir close to EU's initial authorisation as COVID-19 treatmentThe European Medicines Agency (EMA) has already recommended the compassionate use of remdesivir, which allows a drug to be administered to ...
- Sun Pharma gets European Medicines Agency nod for TobramycinThe approval for the product was received by company's wholly owned subsidiary firm from the European Medicines Agency, Sun Pharmaceutical ...
- Germany suspends marketing of 54 drugs tested by GVK BiosciencesGermany's drug regulator has suspended the marketing of 54 medicines clinically tested by India's GVK Biosciences in compliance.
- EU bans 700 generic drugs for manipulation of trials by GVK BiosciencesMedicines affected by the sales ban will lose their validity for use in the EU and they should no longer be sold by pharmaceutical companie...
- German regulator hails European Medicine Agency's drugs suspension on GVK Bio dataThe German watchdog said it will take a decision shortly on whether to add more medicines to the list of banned drugs in the wake of the EM...
- EU regulator recommends suspension of drugs over GVK Bio dataThe recommendation is based on findings from an inspection that raised concerns about how GVK conducted studies at the Hyderabad site on be...
- Four European Union countries suspend authorisation of 25 drugs studied at GVK BiosciencesEuropean Medicines Agency (EMA) said in a statement that it is reviewing findings of non-compliance with good clinical practise at the GVK ...
- European Commission set to approve first drug based on gene therapyThe idea was conceived in the 1970s but after that, a large number of clinical trials did not result in a commercial drug.
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