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A month inside Europe's medicine review process

Original: A month inside Europe’s medicine review process

A detailed look at how the European Medicines Agency and national regulators assess new medicines over the course of a month. The reporting examines how expert committees weigh clinical trial data, safety concerns and manufacturer submissions before deciding whether a drug can be sold in the EU. It offers an inside view of a process that rarely receives sustained public scrutiny.

Why now: Readers are interested in how drug approvals and safety decisions are made in Europe, particularly where new treatments are concerned.

European Medicines AgencyEuropean Union

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