Events

This full-day workshop is designed to provide an introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Porfolio studies conducted within Secondary Care (primarily hospital based) settings.

This Cancer Researchers Introductory Course (CRIC) is taking place at CRN Wessex.

This course is for experienced research delivery staff who - have previously completed either taught or on-line Good Clinical (GCP) training, have recent practical experience of working in a clinical research environment and have a good understanding of the principles and quality standards of GCP and related frameworks.

This full-day workshop is designed to provide an introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Portfolio studies conducted within Secondary Care (primarily hospital based) settings.

This full-day workshop is designed to provide an introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Portfolio studies conducted within Secondary Care (primarily hospital based) settings.

The Informed Consent workshop has been designed to enable attendees to embed the core principles of informed consent into their practice. The materials, developed by a group of Lead Nurses throughout the Clinical Research Network (CRN) aim to provide a foundation upon which to build completence in the informed consent process in a research setting. Locally delivered workshops take the form of a combination of presentations, discussions and group activities designed to bring the principles of informed consent into the workplace.

This full-day workshop is designed to provide an introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Portfolio studies conducted within Secondary Care (primarily hospital based) settings.

This course is for experienced research delivery staff who - have previously completed either taught or on-line Good Clinical (GCP) training, have recent practical experience of working in a clinical research environment and have a good understanding of the principles and quality standards of GCP and related frameworks.

This course is for experienced research delivery staff who - have previously completed either taught or on-line Good Clinical (GCP) training, have recent practical experience of working in a clinical research environment and have a good understanding of the principles and quality standards of GCP and related frameworks.

This course is for experienced research delivery staff who - have previously completed either taught or on-line Good Clinical (GCP) training, have recent practical experience of working in a clinical research environment and have a good understanding of the principles and quality standards of GCP and related frameworks.

This course is designed for those working as a Principal Investigator (PI) or wishing to become a PI and is particularly suited to those who have been working in this role for less than 6 months. The course will focus on the role and responsibilities of the PI, developing a greater understanding of the regulatory landscape in research, leadership, oversight and communication skills and the importance of building working relationships with local R&D and R&I departments.

This full day workshop is designed to provide an introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Portfolio studies conducted within Secondary Care (primarily hospital based) settings.

The Informed Consent workshop has been designed to enable attendees to embed the core principles of informed consent into their practice. The materials, developed by a group of Lead Nurses throughout the Clinical Research Network (CRN) aim to provide a foundation upon which to build completence in the informed consent process in a research setting. Locally delivered workshops take the form of a combination of presentations, discussions and group activities designed to bring the principles of informed consent into the workplace.

The Informed Consent workshop has been designed to enable attendees to embed the core principles of informed consent into their practice. The materials, developed by a group of Lead Nurses throughout the Clinical Research Network (CRN) aim to provide a foundation upon which to build completence in the informed consent process in a research setting. Locally delivered workshops take the form of a combination of presentations, discussions and group activities designed to bring the principles of informed consent into the workplace.

This full-day workshop is designed to provide an Introduction to Good Clinical Practice (GCP), the EU Directives, UK Regulations and Research Governance Framework requirements covering clinical trials and other NIHR Portfolio studies conducted within Secondary Care (primarily hospital based) settings.