Human Medicines Evaluation

The European Medicines Agency's Human Medicines Evaluation Division is responsible for activities related to the scientific, regulatory and procedural management of human medicines evaluation.

This includes ensuring that the evaluation of submissions is performed in a timely manner and with the highest-possible quality.

An organisation chart shows the full structure of the PDF iconHuman Medicines Evaluation Division.

Head of Human Medicines Evaluation

Scientific and Regulatory Management

Procedure Management

How useful was this page?

Add your rating