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Medicine agency: Roche did not report side effects | The Seattle...
www.seattletimes.com
The European Medicines Agency is investigating
First ever gene therapy treatment recommended by European regulator |...
www.foxnews.com
The European Medicines Agency is recommending the first-ever approval of a gene therapy treatment in the EU, in a significant move for a type of treatment that...
EU agency questions AstraZeneca over heart drug trial - Reuters
www.reuters.com
Europe's medicines regulator has written to AstraZeneca asking it to provide more information about a U.S. probe into a clinical trial of the company's new...
Harvard Public Relations baut Consumer- und Coportate-PR-Aktivitäten...
www.horizont.net
Das ehemalige Team der geschlossenen Münchner PR-Agentur More Relations verstärkt
ab sofort unter der Unit-Leitung von Stephan Becker-Sonnenschein den Bereich...
After Brexit Shock, Drug Companies Try To Keep Britain Tied To Europe
www.buzzfeednews.com
Britain’s giant drug companies are not pleased with the referendum result, not least because Europe’s drug regulation agency will have to leave its London...
EMA’s Draft Rules for Interferon Beta Biosimilars Include Clinical...
www.genengnews.com
Guidance is now open to comments and a final rule is expected by the middle of this year.
Morning After Pill Doesn't Work in Heavy Women: Study | Newsmax.com
www.newsmax.com
The morning-after emergency birth control pill may be less effective in heavy women, says a European agency.
Morning-after pill may not work in heavy women | ABC7 San Francisco |...
abc7news.com
The European Medicines Agency says it has started a review of emergency contraceptives to see if they work less well in heavy women
Press Release: Workshop on chordoma discusses challenges of drug...
www.rarecancerseurope.org
Workshop on chordoma discusses challenges of drug development for rare cancers
Roche probed by European regulators for not reporting side effects -...
www.cbsnews.com
Regulators said 80,000 reports by of possible side effects to drugs sold in the U.S. had not been properly analyzed
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