Verification of the compliance of promotional and institutional activities in accordance with the requirements of laws, ethics codes, corporate internal procedures
Regulatory and medical evaluation of promotional and non-promotional materials (disease awareness and institutional including press releases and documentation for market research), specialized press, websites, conferences, etc
Regulatory and medical evaluation of materials to be used by corporate figures such as Medical Science Liaisons, Regional Account Managers
Writing, revision and updating of local standard operating procedures
Support in the main areas of risk related in particular to the collaboration with HCP, HCO, scientific societies, patient associations, etc
Submission of promotional materials to AIFA and follow up in case of requests
Congresses: 360-degree management of authorization procedures, including of relationships with ECM providers and secretariats, submission of the requests for authorization through the AIFA Front End system, follow up until approval and submission of final balance costs of the event
Support for the registration of sales force to regions, notification to AIFA and to Regions of sales force activities
