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03 February 2010 /Authorisation and supervision
Licensing of medicines – prioritisation and forecast processing times for the first half of 2010
The changed administrative procedure that was introduced for national applications in the summer of 2009 now works routinely and according to plan.
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03 February 2010 /Authorisation and supervision
Compliance check of package leaflets and product labelling (winter 2009/2010)
In response to complaints and reports, etc. submitted to the Danish Patient Safety Database, the Danish Medicines Agency has examined different elements of the labelling of the below listed medicinal products to find out whether they comply with the provisions of the executive order on labelling
