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Experienced clinical researchers with prior knowledge of GCP who wish explore the wider application and gain a more in-depth understanding of theÂ regulatory aspects of clinical research.
This course provides an in-depth look at the regulatory systems currently in operation in the EU and their impact, together with UK legislation, on the conduct of clinical research. Starting with a refresher on the history of medicinal product regulations and the need for ethics, the course explains in more detail the practical applications of GCP and outlines recent major developments in GCP. It also explores the impact of EU data protection laws on clinical research and summarises other current issues that affect clinical trials.
Delegates will receive a complimentary copy of the ICH GCP guidelines and a workbook.
Member 450 GBP, Non Member 550 GBP, Discounts for those working in the NHS or Academia