UHB 006 - Data Protection Guidance for Researchers
UHB 040 - Investigational Medicinal Product (IMP) Management Standard Operating Procedure - EQIA
UHB 099 - Research Governance Policy and EQIA
UHB 121 - Archiving of Clinical Trial and Research Study Data: Standard Operating Procedure
UHB 145 - Investigating and Handling Allegations of Research Misconduct Procedure
UHB 146 - Research and Development Human Resource Arrangements for Researchers Working in the NHS
UHB 147 - Informed Consent in Clinical Research
UHB 235 - Managing Breaches of Good Clinical Practice or the Study Protocol - Standard Operating Procedure
UHB 236 - Research Audit Standard Operating Procedure
UHB 247 - Oversight and Monitoring in Research Standard Operating Procedure
UHB 302 - Managing Amendments for UHB Sponsored Research - Standard Operating Procedure
UHB 317 - Training Requirements for Research Staff, including Good Clinical Practice (GCP)
UHB 406 - Reporting Requirements for Cardiff and Vale UHB Sponsored Research: Standard Operational Procedure
UHB 448 - Obtaining Capacity and Capability Confirmation for Research to Start
UHB 449 - Data Management for Clinical Trials - Standard Operating Procedure
UHB 457 - Research Governance Standard Operating Procedure
UHB 461 - Human Tissue in Clinical Research Management Procedure
UHB 475 - Research and Development Strategy 2020 - 2023
UHB 487 - Financial Procedure for Supporting Non-Commercial Research
UHB 524 - Vendor Assessment in Clinical Research Standard Operating Procedure