EEA-Lex

With EEA-Lex you can find information about proposed EU legal acts with possible EEA relevance, adopted EU acts under consideration for incorporation into the EEA Agreement, and acts that have already been incorporated into the Agreement.

Searching in English gives the widest results. You can refine your research results by using the categories in the right-hand column.

Advanced Search

Council Directive 93/39/EEC of 14 June 1993 amending Directives 65/65/EEC, 75/818/EEC and 75/319/EEC in respect of medicinal products
Richtlinie 93/39/EWG des Rates vom 14. Juni 1993 zur Änderung der Richtlinien 65/65/EWG, 75/318/EWG und 75/319/EWG betreffend Arzneimittel
Tilskipun ráðsins 93/39/EBE frá 14. júní 1993 um breytingu á tilskipunum ráðsins 65/65/EBE, 75/318/EBE og 75/319/EBE um lyf
Rådsdirektiv 93/39/EØF av 14. juni 1993 om endring av direktiv 65/65/EØF, 75/318/EØF og 75/319/EØF om legemidler
Council Directive 93/40/EEC of 14 June 1993 amending Directive 81/851/EEC and on the approximation of the laws of the Member States relating to veterinary medicinal products
Richtlinie 93/40/EWG des Rates vom 14. Juni 1993 zur Änderung der Richtlinien 81/851/EWG und 81/852/EWG zur Angleichung der Rechtsvorschriften der Mitgliedstaaten über Tierarzneimittel
Tilskipun ráðsins 93/40/EBE frá 14. júní 1993 um breytingu á tilskipun 81/851/EBE og 81/852/EBE um samræmingu laga aðildarríkjanna um dýralyf
Rådsdirektiv 93/40/EØF av 14. juni 1993 om endring av direktiv 81/851/EØF og 81/852/EØF om tilnærming av medlemsstatenes lovgivning om veterinærpreparater
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
Verordnung (EWG) Nr. 2309/93 des Rates vom 22. Juli 1993 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Schaffung einer Europäischen Agentur für die Beurteilung von Arzneimitteln
Reglugerð ráðsins (EBE) nr. 2309/93 frá 22. júlí 1993 um málsmeðferð bandalagsins við veitingu leyfa fyrir lyfjum sem ætluð eru mönnum og dýrum og eftirlit með þeim og um stofnun Lyfjamálastofnunar Evrópu
Rådsforordning (EØF) nr. 2309/93 av 22. juli 1993 om fastsettelse av framgangsmåter i Fellesskapet for godkjenning og overvåking av legemidler for mennesker og dyr og om opprettelse av et europeisk kontor for legemiddelvurdering
Commission Regulation (EC) No 542/95 of 10 March 1995 concerning the examination of variations to the terms of a marketing authorization falling within the scope of Council Regulation (EEC) No 2309/95
Verordnung (EG) Nr. 542/95 der Kommission vom 10. März 1995 über die Prüfung von Änderungen einer Zulassung gemäß der Verordnung (EWG) Nr. 2309/93 des Rates
Reglugerð framkvæmdastjórnarinnar (EB) nr. 542/95 frá 10. mars 1995 um umfjöllun um breytingar á skilmálum markaðsleyfis sem fellur undir gildissvið reglugerðar ráðsins (EBE) nr. 2309/93
Kommisjonsforordning (EF) nr. 542/95 av 10. mars 1995 om behandling av endringer i vilkårene for markedsføringstillatelser for legemidler i henhold til rådsforordning (EØF) nr. 2309/93
Commission Regulation (EEC) No 895/93 of 16 April 1993 amending Annexes I, II and III of Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Verordnung (EWG) Nr. 895/93 der Kommission vom 16. April 1993 zur Änderung der Anhänge I, II und III der Verordnung (EWG) Nr. 2377/90 des Rates zur Schaffung eines Gemeinschaftsverfahrens für die Festsetzung von Höchstmengen für Tierarzneimittelrückstände in Nahrungsmitteln...
Commission Directive 93/46/EEC of 22 June 1993 replacing and modifying the Annexes to Council Directive 92/109/EEC on the manufacture and placing on the market of certain substances used in the illicit manufacture of narcotic drugs and psychotropic substances
Richtlinie 93/46/EWG der Kommission vom 22. Juni 1993 die die Anhänge der Richtinie 92/109/EWG des Rates über die Herstellung und das Inverkehrbringen bestimmter Stoffe, die zur unerlaubten Herstellung von Suchtstoffen und psychotropen Substanzen verwendet werden, ersetzt und...

Disclaimer: EEA-Lex is provided for information purposes only. The information is not guaranteed or promised to be current or complete and is not intended to replace any applicable legal sources.

Seminar on the European Economic Area - Brussels 17 September 2019