Regulation (EU) 2022/839 of the European Parliament and of the Council of 30 May 2022 laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised or registered in accordance with Directive 2001/82/EC or Regulation (EC) No 726/2004
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Incorporated into the EEA Agreement but no longer in force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.XIII Medicinal Products
Joint committee decision (JCD)
278/2022
In force in the EEA
Yes
Legal Documents
Regulation (EU) 2022/839 of the European Parliament and of the Council of 30 May 2022 laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised or registered in accordance with Directive 2001/82/EC or Regulation (EC) No 726/2004
Reglugerð Evrópuþingsins og ráðsins (ESB) 2022/839 frá 30. maí 2022 um umbreytingarreglur vegna umbúða og merkinga dýralyfja sem eru leyfð eða skráð í samræmi við tilskipun 2001/82/EB eða reglugerð (EB) nr. 726/2004
Verordnung (EU) 2022/839 des Europäischen Parlaments und des Rates vom 30. Mai 2022 zur Festlegung von Übergangsbestimmungen für die Verpackung und Kennzeichnung von Tierarzneimitteln, die gemäß der Richtlinie 2001/82/EG oder der Verordnung (EG) Nr. 726/2004 zugelassen oder registriert wurden
Europaparlaments- og rådsforordning (EU) 2022/839 av 30. mai 2022 om fastsettelse av overgangsregler for emballering og merking av legemidler til dyr som er godkjent eller registrert i samsvar med direktiv 2001/82/EF eller forordning (EF) nr. 726/2004
History
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