EMA, FDA Get Together On Drugs Eligible For PRIME And Breakthrough Designation

Regulators will share ideas on how to facilitate parallel discussions on products submitted under PRIME and breakthrough.

The European Medicines Agency and the US Food and Drug Administration are looking at ways to exchange notes on drugs that become eligible for their respective schemes on speeding access to new innovative medicines, that is, Priority Medicines (PRIME) in the EU and breakthrough therapy designation in the US.

The exercise involves considering how to facilitate parallel discussion on medicines admitted under PRIME and those that receive breakthrough therapy designation to support the

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