Around Decision 2013/455
Citations, amendments, and UK copies of EU law. Bigger circles are relied on more.
Citations, amendments, and UK copies of EU law. Bigger circles are relied on more.
70 laws and 69 links: citations, amendments, and UK copies of EU law. Bigger circles are relied on more.
| Law | Links on map | Importance |
|---|---|---|
| EUTFEU | 1 | 13.88 |
| EUDirective 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use | 1 | 0.25 |
| EUDirective 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products | 1 | 0.18 |
| EUDirective 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products Text with EEA relevance | 1 | 0.17 |
| EURegulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products (recast) (Text with EEA relevance) | 1 | 0.17 |
| EURegulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance) | 1 | 0.15 |
| EUDecision 2013/455 | 69 | 0.00 |
| EUDirective 2012/26/EU | 1 | 0.00 |
| EUCommission Regulation (EU) No 488/2012 | 1 | 0.00 |
| EUCommission Regulation (EU) No 483/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 406/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 394/2013 | 1 | 0.00 |
| EUCommission Regulation (EU) No 344/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 198/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 116/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 115/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 59/2013 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 1191/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 1186/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 1161/2012 | 1 | 0.00 |
| EUCommission Regulation (EU) No 722/2012 | 1 | 0.00 |
| EUCommission Regulation (EU) No 712/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 466/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 436/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 222/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 221/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 202/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 201/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 123/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 122/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 107/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 86/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 85/2012 | 1 | 0.00 |
| EUCommission Implementing Regulation (EU) No 84/2012 | 1 | 0.00 |
| EUCouncil Directive 93/42/EEC of 14 June 1993 concerning medical devices | 1 | 0.00 |
| EURegulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medicinal products for paediatric use and amending Regulation (EEC) No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA relevance) | 1 | 0.00 |
| EURegulation (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 (Text with EEA relevance) | 1 | 0.00 |
| EURegulation (EC) No 596/2009 of the European Parliament and of the Council of 18 June 2009 adapting a number of instruments subject to the procedure referred to in Article 251 of the Treaty to Council Decision 1999/468/EC with regard to the regulatory procedure with scrutiny — Adaptation to the regulatory procedure with scrutiny — Part Four | 1 | 0.00 |
| EUCouncil Regulation (EEC) No 1768/92 of 18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products | 1 | 0.00 |
| EUDirective 2002/98/EC of the European Parliament and of the Council of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components and amending Directive 2001/83/EC | 1 | 0.00 |
| EURegulation (EC) No 1882/2003 of the European Parliament and of the Council of 29 September 2003 adapting to Council Decision 1999/468/EC the provisions relating to committees which assist the Commission in the exercise of its implementing powers laid down in instruments subject to the procedure referred to in Article 251 of the EC Treaty | 1 | 0.00 |
| EUCouncil Regulation (EEC) No 2377/90 of 26 June 1990 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin | 1 | 0.00 |
| EUDirective 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use | 1 | 0.00 |
| EU1999/468/EC: Council Decision of 28 June 1999 laying down the procedures for the exercise of implementing powers conferred on the Commission | 1 | 0.00 |
| EURegulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance ) | 1 | 0.00 |
| EURegulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products Text with EEA relevance | 1 | 0.00 |
| EUDirective 2007/47/EC of the European Parliament and of the Council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market (Text with EEA relevance) | 1 | 0.00 |
| EUDirective 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices | 1 | 0.00 |
| EURegulation (EC) No 219/2009 of the European Parliament and of the Council of 11 March 2009 adapting a number of instruments subject to the procedure referred to in Article 251 of the Treaty to Council Decision 1999/468/EC with regard to the regulatory procedure with scrutiny — Adaptation to the regulatory procedure with scrutiny — Part Two | 1 | 0.00 |
| EUDirective 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells | 1 | 0.00 |
| EUDirective 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance) | 1 | 0.00 |
| EUDirective 2004/24/EC of the European Parliament and of the Council of 31 March 2004 amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use | 1 | 0.00 |
| EUCouncil Regulation (EC) No 297/95 of 10 February 1995 on fees payable to the European Agency for the Evaluation of Medicinal Products | 1 | 0.00 |
| EUCommission Regulation (EC) No 507/2006 of 29 March 2006 on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance) | 1 | 0.00 |
| EURegulation (EC) No 141/2000 of the European Parliament and of the Council of 16 December 1999 on orphan medicinal products | 1 | 0.00 |
| EUCommission Regulation (EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance) | 1 | 0.00 |
| EUDirective 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use Text with EEA relevance | 1 | 0.00 |
| EUCouncil Directive 89/105/EEC of 21 December 1988 relating to the transparency of measures regulating the prices of medicinal products for human use and their inclusion in the scope of national health insurance systems | 1 | 0.00 |
| EUCouncil Directive 76/768/EEC of 27 July 1976 on the approximation of the laws of the Member States relating to cosmetic products | 1 | 0.00 |
| EUDirective 2008/112/EC of the European Parliament and of the Council of 16 December 2008 amending Council Directives 76/768/EEC, 88/378/EEC, 1999/13/EC and Directives 2000/53/EC, 2002/96/EC and 2004/42/EC of the European Parliament and of the Council in order to adapt them to Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2003/1/EC of 6 January 2003 adapting to technical progress Annex II to Council Directive 76/768/EEC on the approximation of the laws of the Member States relating to cosmetic products (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2008/88/EC of 23 September 2008 amending Council Directive 76/768/EEC, concerning cosmetic products, for the purpose of adapting Annexes II and III thereto to technical progress (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Regulation (EC) No 658/2007 of 14 June 2007 concerning financial penalties for infringement of certain obligations in connection with marketing authorisations granted under Regulation (EC) No 726/2004 of the European Parliament and of the Council | 1 | 0.00 |
| EUCommission Directive 2003/12/EC of 3 February 2003 on the reclassification of breast implants in the framework of Directive 93/42/EEC concerning medical devices (Text with EEA relevance) | 1 | 0.00 |
| EUCouncil Directive 93/68/EEC of 22 July 1993 amending Directives 87/404/EEC (simple pressure vessels), 88/378/EEC (safety of toys), 89/106/EEC (construction products), 89/336/EEC (electromagnetic compatibility), 89/392/EEC (machinery), 89/686/EEC (personal protective equipment), 90/384/EEC (non-automatic weighing instruments), 90/385/EEC (active implantable medicinal devices), 90/396/EEC (appliances burning gaseous fuels), 91/263/EEC (telecommunications terminal equipment), 92/42/EEC (new hot-water boilers fired with liquid or gaseous fuels) and 73/23/EEC (electrical equipment designed for use within certain voltage limits) | 1 | 0.00 |
| EUCommission Directive 2009/9/EC of 10 February 2009 amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2005/52/EC of 9 September 2005 amending Council Directive 76/768/EEC, concerning cosmetic products, for the purposes of adapting Annex III thereto to technical progress (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2005/28/EC of 8 April 2005 laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use (Text with EEA relevance) | 1 | 0.00 |
| EUDirective 2004/9/EC of the European Parliament and of the Council of 11 February 2004 on the inspection and verification of good laboratory practice (GLP) (Codified version) (Text with EEA relevance) | 1 | 0.00 |