| 14 December 2015 |
From 1 January 2016, it will be mandatory to use the eAF to apply for marketing authorisations, renewals and variations. This applies to both human and veterinary medicinal products, and it applies to all procedure types.
| 08 December 2015 |
The November issue of Danish Pharmacovigilance Update with news from the EU, the Danish Medicines Agency and short news.