This practice groups Pharegis resources for medical-device registration and related evidence and certification questions. The technical materials address registration pathways, classification and documentation requirements within the Russian and EAEU regulatory context.
Detailed regulatory articles are listed below and retain their established URLs.
Technical library
Registration, evidence and certification guidance
Regulatory support for medical device registration and clinical evidence in Russia and EAEU, from classification and technical files to authorization.
Overview of certification and declaration requirements for medicinal products and medical devices in Russia, with regulatory support from Pharegis.
