The pharmaceutical industry is undergoing many regulatory changes. Those of us involved in research are directly affected. When carrying out our duties there is a risk of compromising the quality of data we generate and of breaching ethical codes. An understanding of the background and the principles of Good Clinical Practice are critical to ensure ethical research, high quality and credible data.

This module describes the key principles and structure of ICH GCP and, by using actual practitioner experience and accounts, provides a broad framework in which to apply the standards of Good Clinical Practice.


Who will benefit from this module?
This course provides essential learning for clinical research associates, project managers and other employees of companies sponsoring clinical research, as well as all healthcare professionals involved in conducting clinical trials. Anyone who needs to develop an understanding of the importance of Good Clinical Practice and its application should take this course.