Regulatory affairs

REGULATORY AFFAIRS

Ensuring your processes comply thanks to a country-wise service.


  • SITE VISITS

    Planning and advice for the organization of visits of manufacturing sites prior to registration.

  • REGISTRATION OF PRODUCTS

    Verification and submission of files to pharmaceutical and medicine departments.

  • VISA RENEWAL

    Renewal of visas and possible alterations such as changes of one or more components, wrapping, flavour, name, formula, analysis process, shelf life, packaging, manufacturing site, etc.

  • MONITORING

    Regulatory, pharmaceutical, customs, administrative (control authorities’ requirements)