Textul licitației

r EU legislation (Regulation (EU) 2017/625 of the European Parliament and of the Council of 15 March 2017), each Member State is required to implement a residue sampling and analysis monitoring plan and to submit their programmes annually to the European Commission for approval. The national legal basis is the European Communities (Control of Animal Remedies and their Residues) Regulations 2009 (S.I. No. 183/2009). The scope of sampling covers various animal/food categories and distinct residue groups such as: - banned substances, - authorised veterinary medicines, - approved animal feed additives (Hereinafter referred to as “Samples”). Samples are required to be analysed at officially approved laboratories holding accreditation to the International Standard ISO 17025:2017. From time to time in conjunction with risk assessment protocols the Department may arrange a survey in relation