Dutch policy for labelling of medicinal products amended

6 November 2017

The Netherlands Medicines Evaluation Board (MEB) has amended the national policy for labelling medicinal products for human use (MEB 6).

As a result of the changes in labelling policy, the policy documents for the Summary of Product Characteristics (SmPC) (MEB 27) and package leaflet (MEB 5) have also been updated.

The MEB held a public consultation on the proposed amendments. The responses were incorporated in the policy document, where possible.

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