Clinical Trials

Clinical Trials for Investigational Medicinal Products SABP/EXECUTIVE BOARD/0010/PROCEDURE01
Clinical Trials - Appendix 1 Roles and Responsibilities of the Trust as a Host SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix G Research Involving Adults Unable to Consent for Themselves SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix 2 Roles and Responsibilities of the Trust as a Research Sponsor SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix 3 Glossary of Terms SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix A Procedure for hosting a clinical trial SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix B Risk Assessment SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix C Guidance for RD Managers in NHS Trusts and Clinical Research In the Pharmaceutical Industry SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix D Costing Industry Sponsored Studies Through the NIHR Networks SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix D1 Copy of the UKCRN Costing Template SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix E Tariff of Charges for NHS Pharmacy Support of Clinical Trials SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix F Informed Consent in Clinical Trials SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix H Role of Pharmacy SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix I NPSA Guidance for Research Ethics Committee in the UK SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix J Algorithm - Is it a Clinical Trial of a Medicinal Product SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix K Clinical Trials Tool Kit SABP/EXECUTIVE BOARD/0010
Clinical Trials - Appendix L Sponsorship Responsibilities in Publicly Funded Trials SABP/EXECUTIVE BOARD/0010
Clinical Trials - Key Points Explained SABP/EXECUTIVE BOARD/0010