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 |
| EUTEU | 1 | 3.73 |
| 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 |
| 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-681/16 Pfizer Ireland Pharmaceuticals, Operations Support Group | 15 | 0.00 |
| EUArne Forsgren v Österreichisches Patentamt (C-631/13) | 1 | 0.00 |
| EUMerck Canada Inc. and Merck Sharp & Dohme Ltd v Sigma Pharmaceuticals plc (C-539/13) | 1 | 0.00 |
| EUEli Lilly and Company Ltd v Human Genome Sciences Inc (C-493/12) | 1 | 0.00 |
| EUMerck & Co. Inc., Merck Sharp & Dohme Ltd and Merck Sharp & Dohme International Services BV v Primecrown Ltd, Ketan Himatlal Mehta, Bharat Himatlal Mehta and Necessity Supplies Ltd and Beecham Group plc v Europharm of Worthing Ltd (C-267/95, C-268/95) | 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 |
| 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 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 |
| 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 |
| EUNovartis AG v Actavis Deutschland GmbH & Co KG and Actavis Ltd (C-574/11) | 1 | 0.00 |
| EUMerck & Co. Inc. v Stephar BV and Petrus Stephanus Exler (C-187/80) | 1 | 0.00 |