Ensuring your processes comply thanks to a country-wise service.
Planning and advice for the organization of visits of manufacturing sites prior to registration.
Verification and submission of files to pharmaceutical and medicine departments.
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.
Regulatory, pharmaceutical, customs, administrative (control authorities’ requirements)