Commission Regulation (EC) No 542/95 of 10 March 1995 concerning the examination of variations to the terms of a marketing authorization falling within the scope of Council Regulation (EEC) No 2309/95
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Incorporated into the EEA Agreement but no longer in force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EU legal act incorporated into the EEA Agreement, but no longer in force in the Agreement
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XIII Medicinal Products
Joint committee decision (JCD)
074/1999
In force in the EEA
No
Legal Documents
Commission Regulation (EC) No 542/95 of 10 March 1995 concerning the examination of variations to the terms of a marketing authorization falling within the scope of Council Regulation (EEC) No 2309/95
Reglugerð framkvæmdastjórnarinnar (EB) nr. 542/95 frá 10. mars 1995 um umfjöllun um breytingar á skilmálum markaðsleyfis sem fellur undir gildissvið reglugerðar ráðsins (EBE) nr. 2309/93
Verordnung (EG) Nr. 542/95 der Kommission vom 10. März 1995 über die Prüfung von Änderungen einer Zulassung gemäß der Verordnung (EWG) Nr. 2309/93 des Rates
Kommisjonsforordning (EF) nr. 542/95 av 10. mars 1995 om behandling av endringer i vilkårene for markedsføringstillatelser for legemidler i henhold til rådsforordning (EØF) nr. 2309/93
History
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