|
No. |
Topic |
Summary |
Pages |
9782
| The EU Clinical Trials and GCP Directives | - | 44 |
9783
| Trial Master File according Eudralex Vol 10 | 13 | 38 |
9784
| Requirements for Investigational Medicinal Products | - | 35 |
9785
| The Management of IMP Supplies | - | 44 |
9786
| Distribution of IMP Supllies | - | 64 |
9787
| Trial-related Inspections | - | 31 |
9788
| Supply and Study Management | 25 | 28 |
9789
| Management of IMPīs for Trials outside the EU | - | 39 |
9790
| Suspected Misconduct and Fraud in Clinical Trials | 23 | 48 |
