Swissmedic & SECO – Expert Consulting for Permits & Special Cases
Healthcare products and dual-use goods are subject to special customs regulations. We reliably guide you through classification, licensing, and authority communications – ensuring your goods reach their destination on time and in full compliance.
Our Services
- Consulting on Swissmedic classification and SECO export permits
- Application processing, verification & compliance documentation
- Coordination with authorities and customs, including risk assessment
- Complete transport coordination, documentation & clearance
Who Needs This?
- Pharmaceutical & MedTech companies (e.g., clinical trials, registration dossiers)
- Exporters of machinery, chemicals, or dual-use products
- SMEs with sensitive product lines (e.g., laboratory equipment, biotech)
Get your non-binding consultation now
Secure your Swissmedic or SECO permits quickly and reliably – our specialists are here to provide personalized guidance.
Frequently Asked Questions about Swissmedic & SECO (FAQ)
When do I need a SECO export permit?
A SECO permit is required for exporting dual-use goods or strategically sensitive products.
Which products require Swissmedic approval?
Medications, active substances, medical devices, certain laboratory products, and narcotics are subject to Swissmedic regulations.
How long does the approval process take?
Processing times range from a few days to several weeks, depending on the product and regulatory requirements.
Can Fischer Global handle the entire process?
While we can guide you through the entire process, registration must be completed by the exporter/importer.