Commission Delegated Regulation (EU) 2022/1644 of 7 July 2022 supplementing Regulation (EU) 2017/625 of the European Parliament and of the Council with specific requirements for 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
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement by a Joint Committee Decision (JCD)
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XII Foodstuffs
Joint committee decision (JCD)
255/2023
In force in the EEA
Yes
Legal Documents
Commission Delegated Regulation (EU) 2022/1644 of 7 July 2022 supplementing Regulation (EU) 2017/625 of the European Parliament and of the Council with specific requirements for 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
Framseld reglugerð framkvæmdastjórnarinnar (ESB) 2022/1644 frá 7. júlí 2022 um viðbætur við reglugerð Evrópuþingsins og ráðsins (ESB) 2017/625 að því er varðar sértækar kröfur um framkvæmd opinbers eftirlits varðandi notkun á lyfjafræðilega virkum efnum sem eru leyfð sem dýralyf eða sem fóðuraukefni ásamt bönnuðum eða óleyfilegum lyfjafræðilega virkum efnum og leifum af þeim
Delegierte Verordnung (EU) 2022/1644 der Kommission vom 7. Juli 2022 zur Ergänzung der Verordnung (EU) 2017/625 des Europäischen Parlaments und des Rates in Bezug auf spezifische Anforderungen an die Durchführung amtlicher Kontrollen der Verwendung pharmakologisch wirksamer Stoffe, die als Tierarzneimittel oder als Futtermittelzusatzstoffe zugelassen sind, und verbotener oder nicht zugelassener pharmakologisch wirksamer Stoffe und der jeweiligen Rückstände
Delegert kommisjonsforordning (EU) 2022/1644 av 7. juli 2022 om utfylling av europaparlaments- og rådsforordning (EU) 2017/625 med særlige krav til gjennomføringen av offentlige kontroller av bruken av farmakologisk virksomme stoffer som er godkjent som legemidler til dyr eller som tilsetningsstoffer i fôr, og restmengder av disse, og av forbudte eller ikke-godkjente farmakologisk virksomme stoffer og restmengder av disse
History
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