To access all the slides from past events, please join as a member.

The information in these resources are the personal opinions of the guest speakers and ICR at the time of presentation. As national regulations and legislation surrounding clinical research are regularly updated, please consult the official guidance before making your own decisions.

1. Welcome slides and ICR Overview – Karen Roy, Co-Chair ICR – Download PDF
2.  MHRA CTIMPs update covering the new notification scheme and route B amendments – Kingyin Lee, Head of Clinical trials, MHRA – Download PDF
3. Managing Applications for Clinical Investigations – Mark Grumbridge – Head of Clinical Investigations Science Research & Innovation Group – Download PDF
4. HRA Update – Kate Greenwood, Senior Improvement Delivery Manager, Health Research Authority – Download PDF
   1. HRA Update Q&As – Download PDF
5. Commercial Research in the NHS and how to build relationships and collaboration with the Life Sciences sector” – Mihaela Sutu, Commercial Research Business Development Manager, University College Hospital NHS Trust – Download PDF
6. The Secure Data Environments – how to access health data for research – view from the North West” – Dr. Sally Stewart, Programme Director, North West SDE – Download PDF
7. GCP Requirements Update & summary of new information since the last GCP and Ethics Forum meeting– Jo Burmester, Director, Clinical Trial Knowhow – Download PDF