Regulation No. 607 on the manufacturing and distribution of medicated feed for animals.

The present Regulation applies to the production and distribution of medicated feed for animals. The Regulation requires that those who manufacture or import medicated feed for animals obtain permission from the Icelandic Medicines Agency to operate. Medicated feed may only be distributed if it is produced from a premix for medicated feed that has been granted marketing authorization in Iceland, or from a premix for medicated feed that has been granted authorization under Article 7(7) of the Medicines Act (No. 93/1994). Manufacturers of medicated feed shall carry out regular quality control of their production, including making appropriate laboratory measurements of the homogeneity of the medicated feed. Medicated feed may only be delivered against a veterinarian's prescription for medicated feed. Prescription forms for medicated feed shall be in accordance with the sample in Appendix 1 to this Regulation.