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Research & Clinical Trial Policies

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 253 - Safety Reporting in Clinical Trials of Investigational Medicinal Products (CTIMPs) 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

UHB 525 - Cardiff Joint Research Office (JRO) Applying for Sponsorships - Non-CTIMPs Standard Operating Procedure (SOP)

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