15 laws and 14 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 |
| 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-237/22 P Mylan IRE Healthcare v Commission | 14 | 0.00 |
| EUAcino AG v European Commission (C-269/13 P) | 1 | 0.00 |
| EUWestfälische Drahtindustrie GmbH and Others v European Commission (C-70/23 P) | 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 847/2000 of 27 April 2000 laying down the provisions for implementation of the criteria for designation of a medicinal product as an orphan medicinal product and definitions of the concepts 'similar medicinal product' and 'clinical superiority' | 1 | 0.00 |
| EUMylan IRE Healthcare Ltd v European Commission (T-303/16) | 1 | 0.00 |
| EUFastweb SpA v European Commission (C-649/21) | 1 | 0.00 |
| EUOpinion of the Advocate General (C-237/22) | 1 | 0.00 |
| EUCouncil Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products | 1 | 0.00 |
| EUCouncil 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 | 1 | 0.00 |
| EUSecond Council Directive 75/319/EEC of 20 May 1975 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products | 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 |