Moreover, most of the existing databases (i.e., OMIM, Human Gene Mutation Database (HGMD), CTD, and PharmGKB ... GPP is Full Member and National Representative at the European Medicines Agency, ...
The reassessment of Leqembi’s safety data follows the agency’s previous recommendation of the drug for use in the EU.
Marketing authorization for the first EU vaccine to protect adolescents against chikungunya has been expedited for its public ...
From 31st January, 2025, all clinical trials in the European Union (EU), including ongoing trials that were approved under the previous legal framework, the Clinical Trials Directive (CTD), are ...
GlobalData on MSN12d
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.
EMA Partners IPO allotment date today: EMA Partners India IPO allotment share allotment will be finalised today (Wednesday, January 22). The investors who applied for the issue can check the EMA ...
The EMA is implementing major changes to accelerate drug approvals in the EU, addressing delays that affect patients and businesses alike. Following a turbulent period marked by Brexit and the ...
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