Puma had a rocky start to this approval, when the drug faced negative opinion from the EMA Committee for Medicinal Products for Human Use (CHMP) in February this year. Data presented to the ...
Southern Living on MSN9d
Soap Nails Are The Southern Grandma-Approved Nail Trend For Spring 2025There has been a gradual swap from the complicated, intensive nail designs that have been trending for the past five years to ...
AUSTRALIAN energy firm, Invictus Energy Limited, has secured an environmental social impact assessment approval from the Zimbabwe Environmental Management Agency (Ema) to begin gas production at ...
The Montreal-based C3i Center obtained regulatory approval from the European Medicine Agency (EMA) to produce cell therapy therapies for the European market. The company obtained a certificate of ...
Takeda (TAK) announced that the EMA has approved an additional two mL pre-filled pen option for Takhzyro for subcutaneous administration in adolescents and adult patients with Hereditary Angioedema.
EMA committee recommends approval of AbbVie’s upadacitinib to treat adults with giant cell arteritis
AbbVie announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending the approval of upadacitinib (Rinvoq; 15 mg, once ...
AstraZeneca’s Imfinzi (durvalumab) in combination with chemotherapy has been recommended for approval in the European Union (EU ... of the European Medicines Agency (EMA) based its positive opinion on ...
An even more major news would be an FDA review, but the EMA is a good second place. In my last coverage, I noted how the company “started” an MAA (the European application for approval over ...
MONTRÉAL, Feb. 19, 2025 (GLOBE NEWSWIRE) — C3i Center (C3i) announces that it has obtained regulatory approval from the EMA (European Medicine Agency) to produce cell therapy treatments for the ...
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