Events at Leicester General Hospital

To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving … Continue reading “GCP training for CTIMP studies”

To gain an understanding of the informed consent process and the practical application of informed consent in research studies involving patients or volunteers. Candidates must have completed GCP training prior to attending this session. This is an interactive workshop based session. If you have access to HELM, course bookings can be accessed via this. For … Continue reading “Consent training”

To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving … Continue reading “GCP training for CTIMP studies”

To gain an understanding of the informed consent process and the practical application of informed consent in research studies involving patients or volunteers. Candidates must have completed GCP training prior to attending this session. This is an interactive workshop based session. If you have access to HELM, course bookings can be accessed via this. For … Continue reading “Consent training”

To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving … Continue reading “GCP training for CTIMP studies”

To gain an understanding of the informed consent process and the practical application of informed consent in research studies involving patients or volunteers. Candidates must have completed GCP training prior to attending this session. This is an interactive workshop based session. If you have access to HELM, course bookings can be accessed via this. For … Continue reading “Consent training”

To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving … Continue reading “GCP training for CTIMP studies”

To gain an understanding of the informed consent process and the practical application of informed consent in research studies involving patients or volunteers. Candidates must have completed GCP training prior to attending this session. This is an interactive workshop based session. If you have access to HELM, course bookings can be accessed via this. For … Continue reading “Consent training”

This training provides a generic guide to creating and maintaining a site file during the lifecycle of that study. Please be aware that anyone who wishes to attend this training must possess a valid GCP certificate. How to book: For further information and to BOOK a place on one of sessions please contact RITraining@uhl-tr.nhs.uk or call 0116 … Continue reading “Site File Management Training”

To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving … Continue reading “GCP training for CTIMP studies”