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CHMP’s March Recommendations Include Dinutuximab, Nonacog Beta Pegol And Trumenba

 
• By John Davis

The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) meets monthly to review applications for centralized EU marketing authorization. Here’s a summary of their March 2017 recommendations.

Europe

The Committee for Medicinal Products for Human Use (CHMP) carries out scientific assessments for the European Medicines Agency and recommends whether medicines submitted through the centralized procedure should be granted marketing authorizations. The committee also prepares scientific and regulatory guidelines and monitors adverse drug reaction reports.

Once approved by the European Commission, a centralized marketing authorization is valid in all EU member states as well as...

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