Regulatory Affairs

➤ Support in registration of medicines, medical devices and supplements

➤ Consulting – different reports, market research, market access, local competition analysis, pharmacovigilance, recommendations and advise

➤ Local legislation interpretation and monitoring

➤ Monitoring and support of imports in order to comply to registered documents

➤ Providing solutions for fast and easy approach in constantly changing market regulations

➤ Active collaboration with authorities in order to improve legal requirements for medicines, sharing experience from other markets