General provisions
Article 3
Member States shall ensure that the part of the MANCP concerning the performance of official controls on the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and of prohibited or unauthorised pharmacologically active substances and residues thereof in live animals and products of animal origin contains the following: (a) a ‘national risk-based control plan for production in the Member States’, as set out in Article 4; (b) a ‘national randomised surveillance plan for production in the Member States’ as set out in Article 5; (c) a ‘national risk-based control plan for third-country imports’ as set out in Article 6.