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Good Clinical Practice and Clinical Trials (An Introduction)

19 February 2015, Berkshire, United Kingdom


Introduction
By the end of the course you will:

•Understand the principles of GCP
•Define the different phases of clinical research
•Understand ethical and regulatory requirements of clinical trials
•Describe the order of events in setting up and running a clinical trial
•List and understand the purpose of the various documents required for a clinical trial
•Understand the interplay between different functions within the sponsoring company when running a clinical trial
•Appreciate the importance of safety reporting within clinical trials
•Define a Serious Adverse Event and a SUSAR

Who should attend:

The course is suitable for people who want a basic introduction to clinical trials and GCP. This may be people who work in a GMP/hospital environment with Investigational Medicinal Products who want a greater understanding of the clinical trials process and documentation requirements. The course is also suitable for those who are about to start a role in clinical research but have not had any formal training. This course provides an introduction to GCP, a more in-depth look at GCP is provided in the “Good Clinical Practice” course.
Venue
The Science and Technology Centre

The Science and Technology Centre, Earley, Whiteknights Road, Reading, Berkshire, RG6 6BZ, United Kingdom

Organised by
Reading Scientific Services Ltd
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