Due to the constantly increasing number of practitioners involved in clinical trials in the Russian Federation it was decided to start practical educational 2-day courses on the rules of Good Clinical Practice (GCP).

Standard GCP («Good Clinical Practice», GOST R 52379-2005) is the international standard of ethics and quality of research trials, that describes the rules for design, conduct, record keeping and reporting on research trials which implies participating of a person as a probationer (clinical trial).

Compliance of the trial with this standard says about public loyalty of research participants, the rules on of their guarantee with safety, longing to not infliction of harm, as well as the requirements for reliability of the trials. These rules have been initiated in the Declaration of Helsinki («Declaration of Helsinki») of International Conference on Harmonization («International Conference on Harmonisation», ICH). Together with the standards of GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) it is designed to standardize some aspects of quality of medical care.

In this course both methods and rules of conduct and organization of clinical studies will be reviewed.
Information about the locations, schedule of seminars will be announced later.

The schedule will appear in this section.