
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 third day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 13 February 2012.
For the Commission
The President
José Manuel BARROSO
ANNEX

The entry for methylprednisolone in Table 1 of the Annex to Regulation (EU) No 37/2010 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
‘Methylprednisolone Methylprednisolone Bovine 10 μg/kg Muscle  Corticoides/Glucocorticoides’
10 μg/kg Fat
10 μg/kg Liver
10 μg/kg Kidney
2 μg/kg Milk
