• europages
  • >
  • COMPANIES - SUPPLIERS - SERVICE PROVIDERS
  • >
  • marketing and export

Results for

Marketing and export - Service Provider - Italy

ItalyService Provider
  1. A-MARKS FACTORY SRL

    Italy

    A-Marks Factory was founded in 2012 with the aim of providing training, consulting and marketing services to companies in an integrated manner in order to achieve the goal of demonstrable outcome of its work. Today A-Marks Factory employs 15 specialists in export, import, marketing, communication and legal. A-Marks Factory has been accredited by the Italian Ministry of Economic Development as one of the companies in Italy that can provide export services to SME’s (small to medium-sized companies) which are financed by EU funding. Our own offices are in Treviso, Milan and Amsterdam A-Marks Factory is offering the following services: STRATEGIC MARKETING Strategic marketing plans, market researches, competition analysis and customer satisfaction analysis BUSINESS DEVELOPMENT Research of potential customers, importers or distributors and trade negotiations COMMUNICATION SERVICES Media planning, press office, organization of (inter)national buyer events and packaging design TRAINING COURSES Focussed on marketing, sales and communication

  2. KLARSONS

    Italy

    The company KLARSONS, is a Service Provider, which operates in the Personnel recruitment, international industry. It also operates in the International trade consultants, International trade consultants, and marketing and export industries. It is based in San Leo, Italy.

  3. FRANCESCO DAL FABRO

    Italy

    The company FRANCESCO DAL FABRO, is a Service Provider, which operates in the Food - import-export industry. It also operates in the import/export service, intermediation for import-export, and marketing and export industries. It is based in Roma, Italy.

  4. MEDIQUASAR CONSULENZA

    Italy

    With the experiences I acquired the following skills: to make/prepare the Clinical Evaluation Based On The Literature, to extension of an existing clinical evaluation ; to resolve the issues concerning the regulatory aspects of: classification of the specific type of the product, CE, marketing authorizations, import / export permits, verify the accuracy of labeling, compliance with the requirements of 'U.S. FDA 510 (k) Medical Device Submissions Requirements, preparation of the technical documentation for medical devices, etc.; to know the requirements on Clinical Investigations; to know the ISO 14155: 2012; to translate.