Our job is to require the approval of your product for its subsequent commercialization

Registration of any products for medical use is a procedure that is carried out by our company in accordance with the requirements of the current local legislation in order to grant permission for medical use of a medicinal product or a permit for the sale of a drug.

• Assessment of eligibility documentation in accordance with local laws
• Identification of a regulatory strategy based on analysis of your product dossier
• Support processes in the authorized bodies
• Project Management
• Interaction with stakeholders involved in the strategy of access products on the market- marketing, supply chain, commercial office