
Article 1 
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Article 2 
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.
It shall apply from 3 July 2013.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 2 May 2013.
For the Commission
The President
José Manuel BARROSO
ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry corresponding to prednisolone is replaced by the following:

Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic classification
‘Prednisolone Prednisolone Bovine 4 μg/kg Muscle NO ENTRY Corticoids/Glucocorticoids’
4 μg/kg Fat
10 μg/kg Liver
10 μg/kg Kidney
6 μg/kg Milk
Equidae 4 μg/kg Muscle
8 μg/kg Fat
6 μg/kg Liver
15 μg/kg Kidney
