On 5 September 2014, the Danish Health and Medicines Authority submitted a draft list of the medicinal products comprised by the new safety measures rules (Directive 2001/83) for consultation.
The consultation period expired on 17 September 2014, and on 3 October we were to inform the European Commission of the medicinal products we recommend including in the common EU lists.
We have received 22 consultation responses.
But on 24 September 2014 the European Commission amended the original guideline for...
Danish Medicines Agency