Description

AimsThis half-day workshop is designed to provide the opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the NHS Research Governance Framework, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS. The workshop also covers practical issues and some scenarios to enhance learning.Expected Learning OutcomesFollowing the course, participants will have a demonstrable understanding of the background and practical implications of the valid informed consent process. This understanding is intended to be a foundation for action about translating principles into practice and give participants the confidence to take a proactive role in the consent process back in the workplace.NB: This course would be useful to anyone involved in the consent process, not just training for those actively receiving consent in practice.BookingThis course is only available to those people who are involved in NIHR research.To book a place please log into or create an account on the NIHR Clinical Research Network’s learning platform, NIHR Learn (https://learn.nihr.ac.uk/) with your NHS or University email.Please access this using your Google Chrome browser. 13 November 201909.00 – 12.30For further Information please email: training.crnthamesvalley@nihr.ac.uk