When a medication has gained approval it still needs to be investigated in day-to-day clinical practice, e.g. concerning its interaction with other agents. IFE Baltic plans and conducts Post-Marketing-Surveillance by providing:

planning in Lithuania, Latvia and Estonia
development plan, development and design of documents including printing, training of representatives, outline of contractual documents, information to relevant authorities

project management
recruitment of physicians, distribution of the documents, registration of data return, status reports, royalties accounting

monitoring
by representatives, telephone contact, professional IFE-monitors or an economic and intelligent combination of all three options

data management
database development, data entry and verification, data validation and query management, documentation of AEs and SAEs, immediate information of sponsor, coding of AEs, concomitant medication, diseases and other items

statistics
biometrical analysis including relevant subgroup analysis, interim evaluation, confirmative, explorative and descriptive statistical techniques, final integrative biometrical and medical report, drafting of publication