Maximise your potential with ICR eLearning

Special offer: Modules only £42 each, or 3 for £84. Limited time only

The ICR clinical research eLearning programme is designed to provide a practical and flexible method for clinical research professionals to learn about aspects of clinical trials.

Can you afford not to invest in your own professional training?

The modules provide an awareness of legislation, current best practice and identify the key issues for a range of areas in clinical research. This enables you to promote good practice and support standards that have the best interests of patients at heart. 

Read about our wide range of interactive modules written by industry experts

• Principles of ICH GCP
• EU Clinical Trials Directive
• ICH GCP for Investigators
• ICH GCP for Sponsors
• Data Protection and Clinical Research in the UK 

• GCP Directive

• Practical Monitoring

• GCP Compliance in Document Management and Archiving

• So you want to be a CRA?

• How to get a job as a CRA

Click on each title for more details on the module content and how you could benefit.

Accessing your modules

If you've already purchased a module, log in with your username and password, click "eLearning access" in the left-hand-side menu and select the correct module to start learning...

Why choose eLearning with ICR?

• Modules distil over 30 years' experience of regulations and guidelines.

• On completing your ICR eLearning module, you will be able to print out a certificate as evidence of having completed a high quality learning programme.

• Earn ICR Continuing Professional Development points while you learn

• Ideal for busy professionals: Start whenever you want, complete over several sessions

l