Opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS.
This workshop is designed to consolidate the key learning from the Introduction to GCP e-learning.
This session is an introduction to the DHSC AcORD guidance and how this is used to assign the costs for research to the appropriate category within an R&D department. This session will focuse on how to complete a SoECAT from an R&D perspective.
Our second Showcase event celebrating the exciting projects working with communities under-served by research.
Opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS.
This training will focus on the roles, responsibilities and much more.
This event will provide a great opportunity to share the latest news from across the region as well as a valuable opportunity for networking, collaboration and career development.
This workshop is designed to consolidate the key learning from the Introduction to GCP e-learning.
The course provides an overview of the basic principles of costs and cost attribution for clinical/health related research and, through some shared group activities, applying the principles to real life research studies.
Opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS.
Two day course aiming to provide foundation of knowledge in order to develop practice as a research practitioner.
Opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS.
This training will focus on the roles, responsibilities and much more.
Opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS.
This workshop is designed to consolidate the key learning from the Introduction to GCP e-learning.