Annex Correlation table
United Kingdom
| Directive 2003/94/EC | This Directive | Commission Delegated Regulation (EU) 2017/1569 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections |
|---|---|---|
| Article 1 | Article 1 | Article 1 |
| Article 2 | Article 2 | Article 2 |
| Article 3 | Article 3 | — |
| Article 4 | Article 4 | Article 3 |
| Article 5 | Article 5 | Article 4 |
| Article 6 | Article 6 | Article 5(1) |
| Article 7 | Article 7 | Article 6 |
| Article 8 | Article 8 | Article 7 |
| Article 9 | Article 9 | Article 8 |
| Article 10 | Article 10 | Article 9 |
| Article 11 | Article 11 | Article 10 |
| Article 12 | Article 12 | Article 13 |
| Article 13 | Article 13 | Article 14 |
| Article 14 | Article 14 | Article 15 |
| Article 15 | — | — |
| Article 16 | — | — |
| Article 17 | — | — |
| Article 18 | — | — |
| Article 19 | — | — |