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Course in GCP

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Course in GCP

Objective

The course within GCP (Good Clinical Practice) provides essential knowledge of the regulations that govern clinical trials, why they exist and how to follow them.

The course is aimed at anyone who works with clinical trials in the
pharmaceutical industry, in the health care system, or others who come into contact with clinical examiners.

The course is mainly directed to those of you who have recently started working in the area or need to update your knowledge of GCP.

The GCP course meets the requirements of the ICH GCP Investigator Site Personal Training that is identified by TransCelerate BioPharma, INC. This is necessary in order to make mutual recognition of GCP training for examiners possible.

Course coordinator and expert: Anders Hellgren, Hellgren GCP Consulting AB

Course content GCP

  • Introduction and background
  • The regulations
  • The research process
  • Research ethics
  • Declaration of Helsinki
  • To conduct a clinical study
  • Ethics and responsibility

Interested in further information?

Welcome to contact Vera Rönngard,  | tel: 070-161 58 49
to order or get more information about the course.

Purchase course