1. Registration of medicines, dietary Supplements and medicinal devices
1.1. Preparation of documentation for medicines registrations, re-newals or variations and processing applications according EU regulations
1.1.1. Regulatory affairs and representing of customer company as the applicant during complete process of preparation for registration and registration procedure in the liable authority.
1.1.2. Organization of (where appropriate) bioequivalence/bioavailability testing, monitoring and documentation preparation including verified clinical overview.