| Title | Number | Version | Release Date |
|---|---|---|---|
| Clinical Trial and Medical Device Risk Assessment Guidance Document | 51.004A | 2.0 | 05/10/22 |
| Non-Compliance Q-Pulse Guide | 51.008A | 1.0 | 19/04/22 |
| Protocol Deviation Guidance | 51.008B | 1.0 | 19/04/22 |
| Guidelines for Identifying Category of Research Funding Organisation | 51.010A | 3.0 | 26/10/22 |
| IMP Manufacturer Vendor Assessment Process | 51.015A | 3.0 | 12/12/18 |
| Use of Q-Pulse for Vendor Assessment Guide | 51.015B | 1.0 | 24/11/21 |
| Quality Control of Trial Master File | 51.016A | 1.0 | 24/07/23 |
| SReDA End Date Process | 51.022A | 2.0 | 14/07/16 |
| Archiving Process Map | 51.024A | 2.0 | 12/04/18 |