Variations and Information Monitoring Sector
- Ensure registration of the received documentation, ensure the preservation of documentation, the flow and circulation of information in the Division, Medicines Marketing Authorization Department and the Pharmacovigilance Division;
- Ensure primary examination/validation of applications for variation to a marketing authorisation and supporting documentation, supervising the coordination of procedures and compliance with deadlines;
- Organise meetings of the Medicines Marketing Authorization Department and the circulation of documentation related to the meetings;
- Ensure the updating of the information on medicinal products in the Medicinal Product Register of Latvia.
