Good Clinical Practice

3 - 4 February 2016, Reading, United Kingdom


Introduction
Course Scope

This course provides an introduction to the clinical trial process and the requirements of Good Clinical Practice GCP. The course will cover each section of ICH-GCP so that participants become familiar with all the guidance. The practical requirements around running a trial to GCP standard will also be covered.

Overview:
At the end of the course you will:
•Understand the principles of GCP
•Be able to define the responsibilities of each party involved in a clinical trial
•Understand ethical issues surrounding informed consent
•Be familiar with each section of ICH-GCP and its contents
•Be able to list and understand the purpose of the various documents required for a clinical trial
•Be able to evaluate your own practice to determine GCP compliance

Who should attend:

The course is suitable for people who have recently started working in clinical trials to ICH-GCP standards. This may be from a sponsor company/sponsor representative e.g. clinical trial leader, study monitor; an investigative site e.g. study physician, study nurse, study coordinator; or review body e.g. hospital research and development committee. The course is also suitable for those who have been previously trained in GCP requiring a refresher.
Venue
RSSL Training

Training room, RSSL Training, The Science and Technology Centre, Earley Gate, Whiteknights Road, Reading, RG6 6BZ, United Kingdom

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