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You have completed 0 of 5 courses in this programme. You can now download your programme certificate.

Course title Access Your grade Certificate

Protocol and Associated Documents (120 mins, 2 CPD pts) Preview Course

Course details

This course is an introduction to the protocol and its associated documents. You will learn about the important sections that you should have in a protocol and this will be followed by the associated documents: the Participant Information Sheets, Consent Forms and Case Report Forms.

Pass mark: 75%
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Applications, Agreements and Approvals (120 mins, 1 CPD pts) Preview Course

Course details

There are an array of regulatory issues, contracts, forms to complete and guidelines to understand in the process of setting up a clinical trial today. This course will guide you through this process.

Pass mark: 75%
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Trial Master Files (120 mins, 1 CPD pts) Preview Course

Course details

This course is designed to help you understand the importance of the Trial Master File (TMF) and how its use and maintenance are essential to carrying out a legally robust and safe clinical trial.

Pass mark: 75%
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Conducting the trial (120 mins, 1 CPD pts) Preview Course

Course details

Once you have started, keeping a trial running well and staying in control and on top of everything, including Good Clinical Practice (GCP) compliance, can be a challenge. This course covers the elements of GCP that are relevant from trial start, through to completion.

Pass mark: 75%
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Safety Reporting (120 mins, 2 CPD pts) Preview Course

Course details

Anyone involved in clinical research will agree that the safety of participants is of paramount importance. Understanding the requirements of the regulations and GCP around safety reporting is essential if you are involved in clinical trials. This course covers all the different aspects of safety reporting that you need to know from protocol development to final reporting.

Pass mark: 75%
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