The European Medicines Agency (EMA) has recommended granting marketing authorization for the pneumococcal vaccine Capvaxive ...
Marketing authorization for the first EU vaccine to protect adolescents against chikungunya has been expedited for its public ...
GlobalData on MSN6d
EU’s Clinical Trials Regulation comes into full forceThe ruling requires all trials across the EU to be filed through the European Medicines Agency’s digital filing system.
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GlobalData on MSNItalian charity seeks EMA approval for rescued gene therapyTelethon Foundation is seeking approval for a gene therapy to treat the rare disease Wiskott-Aldrich syndrome.
In the latest development, the European Commission has asked the EMA's human medicines committee, the CHMP, to take a look at ...
Fondazione Telethon, an Italian biomedical charity focused on rare genetic diseases, has submitted a Marketing Authorization ...
The two products, both manufactured by Amgen, are aflibercept biosimilars Pavblu and Skojoy. Both biosimilars are indicated ...
AstraZeneca (AZN) stock in focus as its partner Daiichi Sankyo (DSNKY) wins EU backing for their jointly developed breast ...
Ocugen (OCGN) announced that the European Commission has provided a positive opinion from the EMA’s, or European Medicines Agency’s, Committee ...
Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the Committee for Medicinal Products ...
The NZD/USD pair breaks its four-day winning streak, trading around 0.5660 during the European hours on Thursday. The ...
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