The registration certification process for a product in the Republic of Armenia consists of several main stages:
Stage 1. Expert preparation of application in consultation with the customer, careful review of application materials ensuring their conformance with the requirements* of medicine registration in the Republic of Armenia.
Stage 2. Preparation of package containing all necessary documents for registration as per the legislation of the Republic of Armenia.
Stage 3. Document submission to the Medicine and Medtech Inspection Scientific Center.
Stage 4. Acquisition of official requests, consultation for additional document preparation in compliance with the authorized bodies’ requirements, and customer advocacy.
Stage 5. Acquisition of registration certificate for the product in the Republic of Armenia.
*When necessary: organizing pre-approval, expert-quality report for the product.