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MU102_10_001i_MB Notifica di vizi di qualità (PDF, 231 kB, 22.12.2025)
MU102_20_001f_MB Commentaires Out of Stock (PDF, 307 kB, 22.12.2025)
BW301_10_001i_FO Domanda importazione stupefacenti sostanze psicotrope precursori (DOCX, 374 kB, 15.12.2025)
OS000_00_008i_MB eIAM Amministratore portale (PDF, 1 MB, 01.11.2025)
BW690_00_001defi_FO Ordine di certificati di esportazione per dispositivi medici (PDF, 1 MB, 01.12.2025)
BW690_00_002i_WL Certificati di esportazione (PDF, 487 kB, 11.12.2025)
ZL105_00_004i_FO Formulario Meeting aziendali per procedure di omologazione (DOCX, 382 kB, 01.12.2025)
I-SMI.TI.18e Legal requirements and mandatory due diligence by Swiss firms wishing to engage in foreign trade with medicinal products or ATMPs from Switzerland, and on supply chain traceability if products are imported for re-export (PDF, 205 kB, 09.12.2025)
BW610_20_021e_FO Modifications, notifications, reports MD IVD (PDF, 1 MB, 18.11.2025)
BW610_20_022e_FO Notification of safety measures MD IVD (PDF, 1 MB, 20.11.2025)
BW610_20_023e_FO SAE-CH and DD-CH MD (PDF, 1 MB, 20.11.2025)
BW610_20_024e_FO SAE-CH and DD-CH IVD (PDF, 1 MB, 20.11.2025)
BW610_20_025e_FO Form Modifications, notifications, reports MD IVD (PDF, 1 MB, 18.11.2025)
BW610_20_026e_FO Notifications of safety measures combined studies (PDF, 1 MB, 20.11.2025)
32_CK_08 Marketing Information Form (PDF, 253 kB, 03.12.2025)
BW690_00_001i_VL Esempio FSC di un elenco di dispositivi e di dispositivi per sistemi e kit procedurali (PDF, 246 kB, 24.11.2025)
MU680_20_815i_WL Guida complementare CH Guida Manufacturer Incident Report (MIR) (PDF, 361 kB, 20.11.2025)
MU103_10_002i_FO Formulario PSUR/PBRER per medicamenti per uso umano (DOCX, 159 kB, 01.12.2025)
ZL000_00_021i_WL Guida complementare Dati sulle confezioni dei medicamenti per uso umano (PDF, 734 kB, 01.12.2025)
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