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52009XC1030(02)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 May 2009 to 31 May 2009 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC )
OJ C 260, 30.10.2009, p. 15–30 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC1030(01)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 September 2009 to 30 September 2009 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council )
OJ C 260, 30.10.2009, p. 6–14 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC0925(04)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 August 2009 to 31 August 2009 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC of the European Parliament and of the Council or Article 38 of Directive 2001/82/EC of the European Parliament and of the Council )
OJ C 231, 25.9.2009, p. 30–37 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC0925(03)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 August 2009 to 31 August 2009 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council )
OJ C 231, 25.9.2009, p. 20–29 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC0925(02)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 July 2009 to 31 July 2009 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC of the European Parliament and of the Council or Article 38 of Directive 2001/82/EC of the European Parliament and of the Council )
OJ C 231, 25.9.2009, p. 18–19 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC0925(01)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 July 2009 to 31 July 2009 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council )
OJ C 231, 25.9.2009, p. 3–17 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XX0923(04)
Opinion of the European Data Protection Supervisor on the proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and on the proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use
OJ C 229, 23.9.2009, p. 19–26 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009PC0486
Opinion of the Commission pursuant to article 251(2), third subparagraph, point (c) of the EC treaty on the European Parliament's amendment to the Council's common position regarding the proposal for a regulation of the European Parliament and of the Council concerning statistics on plant protection products, amending the proposal of the Commission pursuant to article 250(2) of the ec treaty
/* COM/2009/0486 final */
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32009L0120
Commission Directive 2009/120/EC of 14 September 2009 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use as regards advanced therapy medicinal products (Text with EEA relevance)
OJ L 242, 15.9.2009, p. 3–12 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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52009XC0731(09)
Summary of Community decisions on marketing authorisations in respect of medicinal products from 1 June 2009 to 30 June 2009 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC )
OJ C 178, 31.7.2009, p. 24–27 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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