Tag Archives: Industry

Labelling in Russian market medical devices

 All medical devices circulating within the territory of the Russian Federation are subject to safety monitoring.  One of the common violations found during such monitoring activities is the failure to identify the device in question. Each medical device should be clearly identified; all sales should be made only under the trade name stated in the marketing authorization document and in

Read more

Meeting of ICMRA

Mikhail Murashko, Head of Roszdravnadzor, attended the 12th Summit of the Regulatory Agencies’ Heads and took part in the annual meeting of the International Coalition of Medicinal Regulatory Agencies (ICMRA). Mikhail Murashko, Head of Roszdravnadzor, attended the 12th Summit of the Regulatory Agencies’ Heads and took part in the annual meeting of the International Coalition of Medicinal Regulatory Agencies (ICMRA),

Read more