[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"norm-eurlex-reg_2018_221-erwgr-5-de":3},{"law":4,"norm_id":14,"norm_key":15,"slug":16,"title":17,"chapter":18,"content":19,"enriched_content":20,"hierarchy":21,"neighbors_before":22,"neighbors_after":32,"citing_decisions":42,"is_thin":43},{"abbreviation":5,"title":6,"source_type":7,"jurisdiction":8,"document_kind":9,"language":10,"attribution":11,"version_date":12,"source_url":13},"reg_2018_221","zur Änderung der Verordnung (EG) Nr. 999\u002F2001 des Europäischen Parlaments und des Rates und der Verordnung (EG) Nr. 882\u002F2004 des Europäischen Parlaments und des Rates hinsichtlich des Referenzlabors der Europäischen Union für transmissible spongiforme Enzephalopathien","eurlex","eu","regulation","de","© Europäische Union, https:\u002F\u002Feur-lex.europa.eu","2025-02-12","https:\u002F\u002Feur-lex.europa.eu\u002Flegal-content\u002FDE\u002FALL\u002F?uri=CELEX:32018R0221",7068359,"ErwGr. 5","erwgr-5",null,"Erwägungsgründe","Die Verordnung (EG) Nr. 999\u002F2001 und die Verordnung (EG) Nr. 882\u002F2004 sollten daher entsprechend geändert werden.","REG_2018_221 - Erwägungsgründe - ErwGr. 5\n\nDie Verordnung (EG) Nr. 999\u002F2001 und die Verordnung (EG) Nr. 882\u002F2004 sollten daher entsprechend geändert werden.",{},[23,26,29],{"norm_key":24,"title":17,"slug":25},"ErwGr. 4","erwgr-4",{"norm_key":27,"title":17,"slug":28},"ErwGr. 3","erwgr-3",{"norm_key":30,"title":17,"slug":31},"ErwGr. 2","erwgr-2",[33,36,39],{"norm_key":34,"title":17,"slug":35},"ErwGr. 6","erwgr-6",{"norm_key":37,"title":17,"slug":38},"ErwGr. 7","erwgr-7",{"norm_key":40,"title":17,"slug":41},"Art. 1","art-1",[],true]