Good Clinical Practice Course

Good Clinical Practice course

Good Clinical Practice | stem cells Main principles of Good Clinical Practice (GCP). ICH-GCP (E6-R2) international guidelines Regulatory acts of the European Union and International Conference of Harmonization (ICH).Responsibilities and the rights of the parties participating in clinical trials. Interaction of Sponsor and Investigator...

Summary:

Good clinical practice provides a framework of principles which aim to ensure the safety of research participants and the integrity and validity of data. This short course aims to provide the researcher with the basic principles of GCP and how these principles can be applied practically in the research setting. The course is aimed at all those involved in clinical research.

Objectives:

Upon completion of this course, you will have an understanding of:

What Good Clinical Practice (GCP) is
The basic principles of GCP
What being ‘GCP’ qualified means and why conducting a study according to GCP is important
The responsibilities of the investigator
How GCP should be adopted in the conduct of clinical research

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Good Clinical Practice (GCP) Training is a key requirement for individuals involved in clinical research, and is designed to ensure that those involved in conducting a trial are qualified by education, training and experience to perform their respective tasks.

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The Good Clinical Practice Certification is designed to give the researcher a basic understanding of the regulations and requirements for research using investigational drugs or devices.