Process Thinking in Clinical Trials

Hosted at: The Institute of Clinical Research Training Suite

Starts On: September 24, 2019

Finishes: September 24, 2019

10

CPD Points

The Course

ICH E6 (R2) has emphasized the importance of risk management in relation to ensuring subject safety and rights as well as data integrity in clinical trials. Understanding, oversight and improving clinical trial processes, is a fundamental way of managing these risks. this course demonstrates ways to map processes, how to measure them and to understand how they might fail. It provides a tool kit for root cause analysis and provides approaches to improve processes so as to minimize risk. Throughout, examples are used from clinical trials and participants are encouraged to practise the skills they learn. 

Learning Objectives

By the end of this course, you will be able to...

  • Understand the relevance of process thinking in clinical trials
  • Learn how to map processes
  • Learn how to review processes for potential weaknesses and develop preventive actions
  • Practise a method of root cause analysis that goes beyond the normal "Five Whys" approach
  • Understanding different types of actions and how to develop actions to help prevent recurrence of issues (CAPA)
  • Understand how metrics can be used to monitor processes

Course Outline

  • ICH E6 (R2) - Process understanding and risk
  • How to map a process
  • Assessing to process for risk
  • What to do when a process goes wrong - corrections and root cause analysis
  • Preventing further failures (CAPA) 
  • Monitoring process health

Course Documentation

To apply for this course, prices are dependent on your membership status:
Acceptance by WorldPay ensures that your place is booked and guaranteed
To pay by invoice please contact ICR on 01628 501700
Guest ICR Member ICR Member (Academic)
Debit card Credit card Debit card Credit card Debit card Credit card
£550.00 £550.00