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♦ Medical Affairs

Production and dissemination of clinical data

  • Identification of scientific, market and competitors needs, in order to optimize products pre launch and launch activities ( R & D Intelligence).
  • Processing of content and finalization of promotional material, including e- detailing; assessment of compliance with the regulations on advertising of medicinal products; corporate and/or REPs training on specific areas/products.
  • Set up, implementation and follow up of Standard Operating Procedures for advertising and promo activities of medicinal products and medical devices, in accordance with national, regional and deontological rules (e.g. review/approval of promotional materials, monitoring and distribution of free samples, gadgets, attendance at congresses and scientific meetings, staff training, preparation to audits, etc.).
  • KOLs management (e.g. Ad Boards).
  • Relationships with Scientific Societies, Public Institutions, Associations and Foundations.
  • Support for the organization, implementation and finalization of Investigator Initiated Studies, including publication.
  • Finalization of scientific programs for congresses and conferences.
  • Issue and crisis management: identification of risk areas, definition of a business plan in the event of a crisis, media training with specialized companies.
  • Identification of licensing (in/out) opportunities.