New procedure for follow up on adverse drugs reaction reports as of 15 December 2014

09 December 2014, Updated 10 December 2014

The Danish Health and Medicines Authority wants a targeted and relevant process for collecting additional information to reports on adverse drug reactions. 

Therefore, we are by 15 December 2014 implementing a new procedure to ensure, that the information requested as follow up will in fact contribute significantly to the scientific evaluation of the case. 

The new procedure is based on well-defined criteria for selection of cases relevant for follow up.


Follow-up on adverse reaction reports

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