Glasgow Clinical Trials Unit

SOPs Forms
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