Introduction To Clinical Trials & Clinical Trials Practice
Hosted at: The Institute of Clinical Research Training Suite
Starts On: November 30, 2021
Finishes: December 02, 2021
30
CPD Points
The Course
An Introduction to Clinical Trials and Clinical Trial Practice, the ICR’s flagship training course, is accredited by Cranfield University. This highly practical course explores the relevance of clinical research in drug development and summarises the ethical and regulatory requirements for clinical trials. It covers clinical trial methodology and summarises the principles of Good Clinical Practice.
The course gives an overview of the various aspects of clinical research and will be of interest to all members of the clinical study team. It uses a combination of lectures, tutorials and group workshops. Delegates receive a comprehensive workbook and a copy of ICH GCP guidelines. The content of the course will equip delegates to sit the ICR Certificate examination.
Learning Objectives
Relate the relevance of clinical trials to the drug development process
Design a simple protocol and draft appropriate case record forms
Demonstrate the basic principles behind the statistical sections of a protocol
Summarise the ethical and regulatory requirements that must be met before a clinical trial commences
Describe the requirements for conducting monitoring visits
Determine the difference between an adverse event and an adverse drug reaction
Outline the audit process and how it fits into the quality system
Compare the differences between drug and device trials
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