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Medical products are subject to mandatory registration and certification in Russia.
A medical device certification is an official document confirming that an item complies with safety standards. The purpose of the certification is to protect consumers from purchasing low-quality products.
BioVitrum has the Registration Department that supports partners at all stages of the product certification process – from collecting all necessary documentation and passing clinical and technical tests to interacting with the inspection authorities and, as a result, obtaining a registration certificate. BioVitrum has expertise in obtaining all kinds of permits for the circulation of products from any risk class suppliers.