九州影院

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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:

鈥nderstand the principles of GCP
鈥efine the different phases of clinical research
鈥nderstand ethical and regulatory requirements of clinical trials
鈥escribe the order of events in setting up and running a clinical trial
鈥ist and understand the purpose of the various documents required for a clinical trial
鈥nderstand the interplay between different functions within the sponsoring company when running a clinical trial
鈥ppreciate the importance of safety reporting within clinical trials
鈥efine 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 鈥淕ood Clinical Practice鈥 course.

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Venue
The Science and Technology Centre

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

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Organised by
Reading Scientific Services Ltd
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