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

In the next two months, all market representatives should become participants in the labeling system.

GMP News

The amendments came into force in the Decree of the Government of the Russian Federation No. 1556 "On approval of the Regulation on the system for monitoring the circulation of medicinal products for human use."

 

 

They are the regulatory document for the adopted law on the ыефпувimplementation of labeling from January 1 to July 1, 2020.

 

The corresponding Decree of the Government of the Russian Federation No. 1954 on amendments to Resolution No. 1556 was published on January 9, 2020 on the website pravo.gov.ru. Prime Minister Dmitry Medvedev signed the document on December 31, 2019.

 

In accordance with the document, by February 15, 2020, medical institutions must submit an application to CRPT for a drug disposal registrar. Producers and importers must apply for a emissions registrar by May 1, 2020.

 

Read full article at pharmvestnik.ru

All news

 
 

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"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.