PTI’s practical 2-day course gives a complete overview of the modern regulatory GCP framework and takes a detailed look at roles and responsibilities in clinical trials. Delegates will take part in exercises demonstrating how to set up a trial site, make the best use of monitoring visits, and detect inconsistencies using documentation and available data. Participants will also learn how to deal with adverse event reporting quickly and efficiently to avoid non-compliance.

Who Will Attend?
This course is particularly beneficial to all those responsible for monitoring and/or QA of clinical trials. This includes representatives of the following departments of sponsors, CROs and academic institutions:
> Clinical QA
> Clinical Operations
> Clinical Research
> Clinical Development
> Study Management

Course Leader
Please call Mark Westlake on +44 (0)20 7915 5665 for information on your course leader.

Registration required:

Yes

Free:

No