farmakologija
Sorodni pojmi:Predpisi EU, ki neposredno veljajo
Veljavnost | Celex | Naslov |
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22000D1109(29) | Sklep Skupnega odbora EGP št. 74/1999 z dne 28. maja 1999, o spremembi Protokola 37 in Priloge II (Tehnični predpisi, standardi, preskušanje in certificiranje) k Sporazumu EGP |
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22001D0065 | Sklep Skupnega odbora EGP št. 65/2001 z dne 19. junija 2001 o spremembi Priloge II (Tehnični predpisi, standardi, preskušanje in certificiranje) k Sporazumu EGP |
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31979R2748 | Uredba Komisije (EGS) št. 2748/79 z dne 6. decembra 1979 o uvrstitvi blaga v tarifno podštevilko 13.03 C III skupne carinske tarife |
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31983H0571 | 83/571/EEC: Council Recommendation of 26 October 1983 concerning tests relating to the placing on the market of proprietary medicinal products |
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31984D0251 | 84/251/EEC: Commission Decision of 3 May 1984 establishing that the apparatus described as 'Perkin- Elmer - Liquid Chromatograph, model Series 2/1 with spectrophotometric detector, model LC-75 and accessories' may not be imported free of Common Customs Tariff duties |
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31985H0435 | 85/435/EEC: Council Recommendation of 16 September 1985 concerning nationals of the Grand Duchy of Luxembourg who hold a diploma in pharmacy conferred in a third State |
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31987H0176 | 87/176/EEC: Council Recommendation of 9 February 1987 concerning tests relating to the placing on the market of proprietary medicinal products |
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31990D0033 | 90/33/EEC: Commission Decision of 14 December 1989 relating to a proceeding under Article 85 of the EEC Treaty (IV/32.202-APB) (Only the French and Dutch texts are authentic) |
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31994D0358 | Sklep Sveta z dne 16. junija 1994 o sprejetju Konvencije o izdelavi Evropske farmakopeje v imenu Evropske skupnosti |
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32001D0571 | 2001/571/EC: Commission Decision of 18 July 2001 on the national provisions notified by Germany in the field of pharmacovigilance (Text with EEA relevance) (notified under document number C(2001) 1974) |
Predpisi EU, ki so predmet prenosa
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31975L0318 | Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products |
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31981L0852 | Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products |
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31985L0432 | Direktiva Sveta z dne 16. septembra 1985 o uskladitvi zakonov in drugih predpisov v zvezi z nekaterimi dejavnostmi na področju farmacije |
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31985L0433 | Direktiva Sveta z dne 16. septembra 1985 o vzajemnem priznavanju diplom, spričeval in drugih dokazil o formalnih kvalifikacijah iz farmacije, vključno z ukrepi za učinkovito uresničevanje pravice do ustanavljanja za nekatere farmacevtske dejavnosti |
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31985L0584 | Direktiva Sveta z dne 20. decembra 1985 o spremembi Direktive 85/433/EGS o vzajemnem priznavanju diplom, spričeval in drugih dokazil o formalnih kvalifikacijah iz farmacije, vključno z ukrepi za učinkovito uresničevanje pravice do ustanavljanja za nekatere farmacevtske dejavnosti, zaradi pristopa Španije in Portugalske |
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31987L0019 | Council Directive 87/19/EEC of 22 December 1986 amending Directive 75/318/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products |
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31987L0020 | Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products |
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31987L0021 | Council Directive 87/21/EEC of 22 December 1986 amending Directive 65/65/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products |
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31991L0412 | Direktiva Komisije z dne 23. julija 1991 o določitvi načel in smernic dobre proizvodne prakse za zdravila za uporabo v veterinarski medicini |
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31992L0026 | Council Directive 92/26/EEC of 31 March 1992 concerning the classification for the supply of medicinal products for human use |
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