FrancophonIA/DGT-Translation_Memory huggingface dataset:
English: A number of pharmacologically active substances are prohibited or currently not authorised under Regulation (EC) No 2377/90, Directive 96/22/EC or Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition [14]. The residues of pharmacologically active substances in products of animal origin arising, in particular, from illegal use or from environmental contamination should be carefully controlled and monitored in accordance with Council Directive 96/23/EC of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products [15], regardless of the origin of the product.
Maltese: Għadd ta’ sustanzi farmakoloġikament attivi huma pprojbiti jew attwalment mhux awtorizzati skont ir-Regolament (KE) Nru 2377/90, id-Direttiva 96/22/KE jew ir-Regolament (KE) Nru 1831/2003 tal-Parlament Ewropew u tal-Kunsill tat-22 ta’ Settembru 2003 dwar l-additivi għall-użu fl-għalf tal-annimali [14] Ir-residwi ta’ sustanzi farmakoloġikament attivi fi prodotti li joriġinaw mill-annimali li jirriżultaw, b’mod partikolari, mill-użu illegali jew minn tniġġis tal-ambjent għandhom ikunu kkontrollati u monitorjati b’attenzjoni skont id-Direttiva tal-Kunsill 96/23/KE tad-29 ta’ April 1996 dwar miżuri għall-monitoraġġ ta’ ċerti sustanzi u residwi tagħhom f’annimali ħajjin u prodotti tal-annimali [15], ikun x’ikun l-oriġini tal-prodott.
English: Detailed rules on the application of this Article shall be adopted. Those measures, designed to amend non-essential elements of this Regulation by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 26(3).
Polish: Szczegółowe przepisy dotyczące stosowania niniejszego artykułu przyjmowane są zgodnie z procedurą regulacyjną połączoną z kontrolą, o której mowa w art. 26 ust. 3.
English: It is recognised that, in certain cases, scientific risk assessments alone cannot provide all the information on which risk management decisions should be based and that other factors relevant to the matter under consideration should legitimately be taken into account, including the technological aspects of food production and the feasibility of controls. The Agency should therefore provide an opinion consisting of a scientific risk assessment and risk management recommendations on residues of pharmacologically active substances.
Romanian: Este recunoscut că, în anumite cazuri, doar evaluarea științifică a riscurilor nu poate furniza toate informațiile pe care ar trebui să se bazeze o decizie de management și că alți factori relevanți pentru domeniul respectiv ar trebui luați în mod legitim în considerare, inclusiv aspectele tehnologice ale producției alimentelor și fezabilitatea controalelor; în consecință, agenția ar trebui să furnizeze un aviz cu privire la evaluarea științifică a riscurilor și recomandări de gestionare a riscului privind reziduurile substanțelor farmacologic active.