medicinske raziskave
Sorodni pojmi:Predpisi EU, ki neposredno veljajo
Veljavnost | Celex | Naslov |
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22000D0615(13) | Sklep Skupnega odbora EGP št. 37/2000 z dne 31. marca 2000 o spremembi Protokola 31 k Sporazumu EGP o sodelovanju na posebnih področjih, za katera ne veljajo štiri temeljne svobode |
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22000D1214(13) | Sklep Skupnega odbora EGP št. 83/2000 z dne 2. oktobra 2000 o spremembi Protokola 31 k Sporazumu EGP o sodelovanju na posebnih področjih, za katera ne veljajo štiri temeljne svobode |
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31983D0239 | 83/239/EEC: Commission Decision of 4 May 1983 establishing that the apparatus described as 'Gilford - Computer-Assisted Analyzer, model System 4' may not be imported free of Common Customs Tariff duties |
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31983D0302 | 83/302/EEC: Commission Decision of 9 June 1983 establishing that the apparatus described as 'Delmar - Electrocardioscanner, model 660A with DCG Data Terminal, model 680, Ambulatory Pressurometer II System and Arrhythmia Analyzer, model 662B' may not be imported free of Common Customs Tariff duties |
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31983D0344 | 83/344/EEC: Commission Decision of 5 July 1983 establishing that the apparatus described as 'Beckman - UV-Vis Spectrophotometer, model 25', may not be imported free of Common Customs Tariff duties |
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31984D0348 | 84/348/EEC: Commission Decision of 20 June 1984 establishing that the apparatus described as 'Browne - Nocturnale Penile Tumescence Monitor, model 9900 with Playback Printer, model 9800' may not be imported free of Common Customs Tariff duties |
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31991D0317 | 91/317/EEC: Decision of the Council and the Ministers for Health of the Member States, meeting within the Council of 4 June 1991 adopting a plan of action in the framework of the 1991 to 1993 ' Europe against AIDS' programme |
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31991D0640 | 91/640/EEC: Commission Decision of 22 November 1991 approving the plan for infectious haemopoietic necrosis and viral haemorrhagic septicaemia submitted by Denmark (Only the Danish text is authentic) |
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31991D0641 | 91/641/EEC: Commission Decision of 26 November 1991 approving the plan for infectious haemopoietic necrosis and viral haemorrhagic septicaemia submitted by Ireland (Only the English text is authentic) |
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31994D0913 | 94/913/EC: Council Decision of 15 December 1994 adopting a specific programme of research and technological development, including demonstration, in the field of biomedicine and health (1994 to 1998) |
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Predpisi EU, ki so predmet prenosa
Veljavnost | Celex | Naslov |
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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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31975L0319 | Second Council Directive 75/319/EEC of 20 May 1975 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products |
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31978L0420 | Council Directive 78/420/EEC of 2 May 1978 amending Second Directive 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to 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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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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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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32005L0028 | Direktiva Komisije 2005/28/ES z dne 8. aprila 2005 o načelih in podrobnih smernicah za dobro klinično prakso v zvezi z zdravili v preskušanju za humano uporabo ter o zahtevah za pridobitev dovoljenja za proizvodnjo ali uvoz takšnih izdelkov . |