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  • 32008R1234

    Commission Regulation (EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance)

     OJ L 334, 12.12.2008, p. 7–24 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)


  • 22004D0003

    Decision of the EEA Joint Committee No 3/2004 of 6 February 2004 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

     OJ L 116, 22.4.2004, p. 44–45 (ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV)


  • 31995R0541

    Commission Regulation (EC) No 541/95 of 10 March 1995 concerning the examination of variations to the terms of a marketing authorization granted by a competent authority of a Member State

     OJ L 55, 11.3.1995, p. 7–14 (ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV)


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