The main purpose of registration is to ensure that the population is provided with safe, effective, and high-quality medicines. During the registration procedure, medicinal products are checked for compliance with the declared characteristics, undergo various tests, pharmaceutical expertise to identify all kinds of risks.
The high professionalism of the staff and extensive experience in Max Farma allow you to quickly find a solution in case of disputes or difficult situations when registering various medical products, medical devices and equipment and dietary supplements.
Services provided by Max Farma:
— Consulting
— Making changes to the registration certificate
— Making changes to the registration dossier
— Preparation and collection of the registration dossier
— Support in testing
— Preparation of documents in accordance with the requirements of the legislation
— Submission of documents to certain regulatory authorities
— Solving various problems in the registration process
Registration steps:
— Preparation and collection of dossier submission of an application to the State body
— Examination of the dossier
— Laboratory tests
— Preclinical trials
— Clinical trials
— Expert assessment of the quality and effectiveness of the medicinal product
— Obtaining a registration certificate
Max Farma provides its services in the countries of Central Asia and the Caucasus, and the stages of registration may be different depending on the country.