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Sökning efter: Europeiska kommissionen
5329 träffar
|
Titel |
Författare |
År |
Språk |
321 |
Pharmaceuticals in the environment - current knowledge and need assessment to reduce presence and impact
|
|
c2010 |
Engelska |
322 |
Integrated tariff of the European Communities - (TARIC)
|
|
1991 |
Engelska |
323 |
Life and resource efficiency - decoupling growth from resource use
|
|
2011 |
Engelska |
324 |
Promoting equality - activities on fighting discrimination in 2009
|
|
2010 |
Engelska |
325 |
The 2012 ageing report - economic and budgetary projections for the 27 EU member states (2010-2060)
|
|
2012 |
Engelska |
326 |
Dissemination of the results of biological studies - studies and support services related to the common fisheries policy : final report
|
|
2004 |
Engelska |
327 |
Arkiven i Europeiska unionen - rapport från Expertgruppen för samordning på arkivområdet
|
Europeiska kommissionen
|
1997 |
Svenska |
328 |
Nitratdirektivet (91/676/EEG) - vattenmiljön och jordbruket : nuvarande situation och utvecklingstendenser : riktlinjer för medlemsstaternas rapporter
|
|
2000 |
Svenska |
329 |
Svenska regioner i Europeiska unionen - en regionalpolitisk översikt
|
|
1995 |
Svenska |
330 |
The rules governing medicinal products in the European Community Vol. 2, Notice to applicants for marketing authorizations for medicinal products for human use in the Member States of the European Communy
|
|
1989 |
Engelska |
331 |
The rules governing medicinal products in the European Community Vol. 4, Guide to good manufacturing practice for medical products
|
|
1989 |
Engelska |
332 |
The rules governing medicinal products in the European Community Vol. 3, Guidelines on the quality, safety and efficacy of medical products for human use
|
|
1989 |
Engelska |
333 |
The rules governing medicinal products in the European Community Vol. 5, Veterinary medicinal products
|
|
1989 |
Engelska |
334 |
The rules governing medicinal products in the European Community Vol. 3. Addendum july 1990, Guidelines on the quality, safety and efficacy of medicinal products for human use
|
|
1990 |
Engelska |
335 |
The rules governing medicinal products in the European Community Vol. 1, The rules governing medicinal products for human use in the European Community
|
|
1991 |
Engelska |
336 |
The rules governing medicinal products in the European Community Vol. 6, Establishment by the European Community of maximum residue limits ( MRLs ) for residues of veterinary medicinal products in foodstuffs of animal origin
|
|
1991 |
Engelska |
337 |
The rules governing medicinal products in the European Community Vol. 4, Good manufacturing practice for medicinal products
|
|
1992 |
Engelska |
338 |
The rules governing medicinal products in the European Community Vol. 3. Addendum No 2, Guidelines on the quality, safety and efficacy of medicinal products for human use
|
|
1992 |
Engelska |
339 |
The rules governing medicinal products in the European Community Vol. 5 A, The rules governing veterinary medicinal products in the European Community
|
|
1993 |
Engelska |
340 |
The rules governing medicinal products in the European Community Vol. 5 B, Notice to applicants for marketing authorization for veterinary medicinal products in the European Community
|
|
1993 |
Engelska |
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