Abstract

The Ministry of Industry and Trade of the Russian Federation has been carrying out inspections of the foreign pharmaceutical manufacturers since April 2016. The inspectorate checks the foreign manufacturer's compliance with the Russian standards of Good Manufacturing Practice (GMP). Inspection is a key element in assessing the compliance of pharmaceutical manufacturers with GMP requirements. Nearly all the inspections identify discrepancies or violations that are documented in the inspection report and serve as a basis for taking regulatory actions such as the decision to issue a GMP-certificate or refuse to issue it, an order to eliminate discrepancies /violations, suspend or cancel a license, a marketing authorization, prohibition of manufacture, etc.

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