Publications about licensing and supervision
| 26 November 2012 |
In 2011, 356 reports of medicinal product defects were registered, which is the highest number ever. The majority of the reports came from companies and other authorities and predominantly concerned defects on the package and packaging material and deviations from specifications.
| 07 June 2012 |
The Danish Health Authority has published its annual report 2011 on applications for clinical trials of medicines in humans.