16 laws and 15 links: citations, amendments, and UK copies of EU law. Bigger circles are relied on more.
| Law | Links on map | Importance |
|---|---|---|
| EUTFEU | 1 | 13.88 |
| EUCharter | 1 | 3.98 |
| 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 |
| EURoquette Frères SA v Direction des services fiscaux du Pas-de-Calais (C-88/99) | 1 | 0.16 |
| EUPigs Marketing Board v Raymond Redmond (83/78) | 1 | 0.16 |
| EUC-492/23 Russmedia Digital and Inform Media Press | 1 | 0.16 |
| 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 |
| EUC-118/24 Laboratoires Eurogenerics and Theramex France | 15 | 0.00 |
| EUOlainfarm AS v Latvijas Republikas Veselības ministrija and Zāļu valsts aģentūra (C-104/13) | 1 | 0.00 |
| EUProceedings brought by Astellas Pharma GmbH (C-557/16) | 1 | 0.00 |
| EURegulation (EU) 2019/5 | 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 |
| EUEG Labo Laboratoires Eurogenerics SAS and Theramex France SAS v Agence nationale de sécurité du médicament et des produits de santé (ANSM) and Biogaran SAS (C-118/24) | 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 |
| 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 |
| 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 |