The Committee is responsible for preparing the European Medicines Agency’s (EMA) opinions on all questions concerning medicinal products for human use, in accordance with Regulation (EC) No 726/2004.
The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended approving ...
The reassessment of Leqembi’s safety data follows the agency’s previous recommendation of the drug for use in the EU.
The two products, both manufactured by Amgen, are aflibercept biosimilars Pavblu and Skojoy. Both biosimilars are indicated ...
HYDERABAD: Pharma biggie Dr Reddy’s Laboratories Ltd on Monday said the European Medicines Agency’s (EMA) committee for medicinal products for human use (CHMP) has recommended its proposed ...
Imfinzi has been recommended for approval in the European Union, EU, as monotherapy for the treatment of adults with ...