Vir - besedilo: 31993L0040 Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products
Sobesedilo: Where the procedure laid down in this Article is to be followed the Commission shall be assisted by the "Standing Committee on Veterinary Medicinal Products".
Vir - besedilo: 31993L0040 Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products, preamble
Sobesedilo: whereas, in the event of a disagreement between Member States about the quality, the safety or the efficacy of a veterinary medicinal product, a scientific evaluation of the matter should be undertaken by the Committee for Veterinary Medicinal Products
Vir - besedilo: 32003R1085 UREDBA KOMISIJE (ES) št. 1085/2003 z dne 3. junija 2003 o pregledu sprememb dovoljenja za promet z zdravili za uporabo v humani medicini in zdravili za uporabo v veterinarski medicini, ki spadajo v področje Uredbe Sveta (EGS) št. 2309/93, uvod (12)
Sobesedilo: Ukrepi, predvideni s to uredbo, so v skladu z mnenjem Stalnega odbora za zdravila za uporabo v humani medicini in Stalnega odbora za zdravila za uporabo v veterinarski medicini
Vir - besedilo: 31993R2309 Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products, preamble
Vir - besedilo: 31993R2309 Uredba Sveta (EGS) št. 2309/93 z dne 22. julija 1993, ki določa postopke Skupnosti za pridobitev dovoljenja za promet in nadzor zdravil za ljudi in za uporabo v veterini ter ustanavlja Evropsko agencijo za vrednotenje zdravil, uvod
Sobesedilo: ker bi glede zdravil za uporabo v veterini ta odgovornost morala biti dodeljena odboru za zdravila za uporabo v veterini, ustanovljenem z Direktivo 81/851/EGS;
Definicija: Any of the monovalent metals lithium, sodium, potassium, rubidium, caesium, and francium, belonging to group 1A of the periodic table. They are all very reactive and electropositive.
Definicija: Enovalentne kovine: litij, natrij, kalij, rubidij, cezij in francij, ki spadajo v skupino 1A periodnega sistema elementov. Vsi so zelo reaktivni in elektropozitivni.
Vir definicije: CED
Vir - besedilo: Tezaver Gemet, https://www.eionet.europa.eu/gemet/sl/about/
Vir - besedilo: 21998A0703(01) AGREEMENT on the implementation of the provisions of the United nations Convention on the Law of the Sea of 10 December 1982 relating to the conservation and management of straddling fish stocks and highly migratory fish stocks, Preamble
Definicija: A browser-compatible form template that has been published to a server running InfoPath Forms Services, and that has been browser-enabled so that users can both display and fill out the form in a Web browser.
Definicija: The Committee may examine any question relating to the application of Council Regulation (EEC) No 348/81 of 20 January 1981 on common rules for imports of whales or other cetacean products, including the question of control. It also delivers its opinion on the draft of the measures to be taken under the above Regulation.
Vir - besedilo: 31997L0023 Directive 97/23/EC of the European Parliament and of the Council of 29 May 1997 on the approximation of the laws of the Member States concerning pressure equipment, Annex I, 2.2.3 b)
Vir - besedilo: 31997L0023 Direktiva 97/23/ES Evropskega parlamenta in Sveta z dne 29. maja 1997 o približevanju zakonodaje držav članic v zvezi s tlačno opremo
Vir - besedilo: 32002D0079 Commission Decision of 4 February 2002 imposing special conditions on the import of peanuts and certain products derived from peanuts originating in or consigned from China (notified under document number C(2002) 385) (Text with EEA relevance) (2002/79/EC), Preamble (10)
Vir - besedilo: 31997R0258 UREDBA (ES) št. 258/97 EVROPSKEGA PARLAMENTA IN SVETA z dne 27. januarja 1997 v zvezi z novimi živili in novimi živilskimi sestavinami
Definicija: The Committee consists of representatives of organizations of industry, consumers, agriculture, commerce and workers. The Committee may be consulted by the Commission on any problems concerning the harmonization of legislation relating to foodstuffs.
Vir - besedilo: 31993L0040 Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products
Sobesedilo: Where the procedure laid down in this Article is to be followed the Commission shall be assisted by the "Standing Committee on Veterinary Medicinal Products".
Vir - besedilo: 31993L0040 Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products, preamble
Sobesedilo: whereas, in the event of a disagreement between Member States about the quality, the safety or the efficacy of a veterinary medicinal product, a scientific evaluation of the matter should be undertaken by the Committee for Veterinary Medicinal Products
Vir - besedilo: 32003R1085 UREDBA KOMISIJE (ES) št. 1085/2003 z dne 3. junija 2003 o pregledu sprememb dovoljenja za promet z zdravili za uporabo v humani medicini in zdravili za uporabo v veterinarski medicini, ki spadajo v področje Uredbe Sveta (EGS) št. 2309/93, uvod (12)
Sobesedilo: Ukrepi, predvideni s to uredbo, so v skladu z mnenjem Stalnega odbora za zdravila za uporabo v humani medicini in Stalnega odbora za zdravila za uporabo v veterinarski medicini
Vir - besedilo: 31993R2309 Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products, preamble
Vir - besedilo: 31993R2309 Uredba Sveta (EGS) št. 2309/93 z dne 22. julija 1993, ki določa postopke Skupnosti za pridobitev dovoljenja za promet in nadzor zdravil za ljudi in za uporabo v veterini ter ustanavlja Evropsko agencijo za vrednotenje zdravil, uvod
Sobesedilo: ker bi glede zdravil za uporabo v veterini ta odgovornost morala biti dodeljena odboru za zdravila za uporabo v veterini, ustanovljenem z Direktivo 81/851/EGS;
Definicija: A Web application running on the Certificate Lifecycle Manager (CLM) server. This component of the CLM server interacts directly with users in a self-service mode. The specific functionality is based upon Active Directory group memberships and permissions. The certificate subscriber and certificate manager Web portals are both accessed through the same universal resource locator (URL); however, the content displayed is based on a user's roles and permissions.