Locations inspection manufacturers

drugs

In compliance with the rules
of good manufacturing practice,
activity which is beyond
outside the Russian Federation.

 

The geography of our audits covers

Russia and CIS countries

Western and Eastern Europe,
countries of Southeast Asia and
the Middle East, India, Japan

Expert Consulting Seminar “Transition to the EAEU GMP Rules”

GMP News

Transition to the EAEU GMP rules.

 

 

FSI “SID and GP” and “PHARMSTRATEGIA” LLC, as part of a joint program to promote the implementation of best practices in the Russian pharmaceutical industry, will conduct a advance training program on January 30-31, 2020 in the form of an open expert consultation on the topic: “Transition to the EAEU GMP rules. Regulatory requirements and regulatory expectations regarding the validation of computer-aided systems. Validation of equipment for labelling".

 

Validation of computer-aided systems is an area in which properly organized interaction of specialists from different departments is especially critical for achieving positive results. The seminar program is designed in such a way as to ensure the study of important aspects of this interaction, and should be equally useful both for employees of quality assurance departments and for specialists of IT departments of pharmaceutical companies.

 

Read full article at gmpevents.ru

All news

 
 

8-495-004-50-76

105064, Moscow, 5 Nizhny Susalny lane, build 19, area XI, room 2

info@gmp-project.ru

Sitemap

"GMP-Project" - a company that specializes in assisting in the preparation of the inspection of manufacturers of medicinal products for compliance with the rules of good manufacturing practice, the activity of which is located outside the Russian Federation.