20 laws and 19 links: citations, amendments, and UK copies of EU law. Bigger circles are relied on more.
| Law | Links on map | Importance |
|---|---|---|
| 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 |
| EUThe Queen, on the application of Generics (UK) Ltd v Licensing Authority (C-527/07) | 19 | 0.00 |
| EUOlainfarm AS v Latvijas Republikas Veselības ministrija and Zāļu valsts aģentūra (C-104/13) | 1 | 0.00 |
| EUT-223/20 Orion v Commission | 1 | 0.00 |
| EUNovartis Europharm Ltd v European Commission (T-472/12) | 1 | 0.00 |
| EUThe Queen v Licensing Authority of the Department of Health and Norgine Ltd, ex parte Scotia Pharmaceuticals Ltd (C-440/93) | 1 | 0.00 |
| EUAstraZeneca A/S v Lægemiddelstyrelsen (C-223/01) | 1 | 0.00 |
| EUThe Queen v The Licensing Authority established by the Medicines Act 1968 (acting by The Medicines Control Agency), ex parte Generics (UK) Ltd, The Wellcome Foundation Ltd and Glaxo Operations UK Ltd and Others (C-368/96) | 1 | 0.00 |
| EUPP Nature-Balance Lizenz GmbH v European Commission (T-189/13) | 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 |
| 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 |
| EUCouncil Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products | 1 | 0.00 |
| EUThe Queen, on the application of Generics (UK) Ltd v Licensing Authority (C-527/07) | 1 | 0.00 |
| EUCouncil Directive 93/39/EEC of 14 June 1993 amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC in respect of medicinal products | 1 | 0.00 |
| EUCommission Directive 1999/83/EC of 8 September 1999 amending the Annex to Council Directive 75/318/EEC on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of medicinal products (Text with EEA relevance) | 1 | 0.00 |
| EUCommission Directive 2000/38/EC of 5 June 2000 amending Chapter Va (Pharmacovigilance) of Council Directive 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to medicinal products (Text with EEA relevance) | 1 | 0.00 |
| EUNovartis Europharm Ltd v European Commission (T-67/13) | 1 | 0.00 |