EMA advances in implementation of transparency policy and publishes new clinical data

Eveline Van Keymeulen

On 19 December 2016, the European Medicines Agency (EMA) issued an updated version of the External guidance on the implementation of EMA Policy 0070 on publication of clinical data for human medicines. A Summary document outlines the main changes introduced by the revision.

As the EMA advances in the implementation of its transparency policy, data on two additional medicinal products (Praxbind and Tarceva) have been made available as of today on the EMA’s dedicated website, which was launched on 20 October 2016.

This post was originally authored by Marco de Morpurgo.

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