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EUV 1252/2014
Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use
Edition
2014-05-28
EU 2015/ECE78 ; ECE R 78:2015-01-30 ; ECE 78:2015-01-30 ; 2015/145:2015-01-30
Regulation No 78 of the Economic Commission for Europe of the United Nations (UNECE) - Uniform provisions concerning the approval of vehicles of categories L1, L2, L3, L4 and L5 with regard to braking
Edition
2015-01-30
EUV 1252/2014Ber
Corrigendum to Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use
Edition
2015-10-06
EUV 2016/161
Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use
Edition
2015-10-02
2001/83/EGGSLeitl ; 2015/C95/01:2015-03-19
Guidelines of 19 March 2015 on principles of Good Distribution Practice of active substances for medicinal products for human use
Edition
2015-03-19
BremsanlHURL
Richtlinie für die Prüfung der Bremsanlagen von Fahrzeugen bei Hauptuntersuchungen (HU) nach § 29 StVZO (HU-Bremsenrichtlinie)
Edition
2012-05-24
2009/53/EG
Directive 2009/53/EC of the European Parliament and of the Council of 18 June 2009 amending Directive 2001/82/EC and Directive 2001/83/EC, as regards variations to the terms of marketing authorisations for medicinal products
Edition
2009-06-18
EnVersSchElektrMagnFeldEmpf
Bekanntmachung einer Empfehlung der Strahlenschutzkommission; Schutz vor elektrischen und magnetischen Feldern der elektrischen Energieversorgung und -anwendung
Edition
2008-05-15
EGV 1394/2007
Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004
Edition
2007-11-13
2001/82/EGLeitl
Guideline on the definition of a potential serious risk to human or animal health or for the environment in the context of Article 33(1) and (2) of Directive 2001/82/EC - March 2006
Edition
2006-06-07