Commission Delegated Regulation (EU) 2022/2239 of 6 September 2022 amending Regulation (EU) No 536/2014 of the European Parliament and of the Council as regards labelling requirements for unauthorised investigational and unauthorised auxiliary medicinal products for human use
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Incorporated into the EEA Agreement but no longer in force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)
007/2023
In force in the EEA
Yes
Legal Documents
Commission Delegated Regulation (EU) 2022/2239 of 6 September 2022 amending Regulation (EU) No 536/2014 of the European Parliament and of the Council as regards labelling requirements for unauthorised investigational and unauthorised auxiliary medicinal products for human use
Framseld reglugerð framkvæmdastjórnarinnar (ESB) 2022/2239 frá 6. september 2022 um breytingu á reglugerð Evrópuþingsins og ráðsins (ESB) nr. 536/2014 að því er varðar kröfur um merkingar á rannsóknarlyfjum og aukalyfjum án markaðsleyfis fyrir menn
Delegierte Verordnung (EU) 2022/2239 der Kommission vom 6. September 2022 zur Änderung der Verordnung (EU) Nr. 536/2014 des Europäischen Parlaments und des Rates hinsichtlich der Etikettierungsanforderungen an nicht zugelassene Prüf- und Hilfspräparate zur Anwendung beim Menschen
Delegert kommisjonsforordning (EU) 2022/2239 av 6. september 2022 om endring av europaparlaments- og rådsforordning (EU) nr. 536/2014 med hensyn til krav til merking av ikke-godkjente utprøvingspreparater og ikke-godkjente tilleggslegemidler til mennesker
History
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