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December 2025

22.12.2025

MU102_10_001e_MB Notification of Quality Defects (PDF, 255 kB, 22.12.2025)

MU102_20_001d_MB Out-of-Stock Situation (PDF, 257 kB, 22.12.2025)

15.12.2025

BW301_10_001d_FO Einfuhrgesuch kontrollierte Substanzen (DOCX, 368 kB, 15.12.2025)

OS000_00_008e_MB eIAM Portal Administrator (PDF, 1 MB, 01.11.2025)

10.12.2025

BW690_00_001defi_FO Orders for export certificates for medical devices (PDF, 1 MB, 01.12.2025)

BW690_00_002e_WL Export Certificates (PDF, 523 kB, 11.12.2025)

ZL105_00_004e_FO Form Meeting for applicants for authorisation procedures (DOCX, 384 kB, 01.12.2025)

09.12.2025

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)

04.12.2025

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)

03.12.2025

32_CK_08 Marketing Information Form (PDF, 253 kB, 03.12.2025)

BW690_00_001e_VL FSC - Examples of a Product List as well as a Product List for Systems and Procedure Packs (PDF, 249 kB, 24.11.2025)

MU680_20_815e_WL Guidance document CH Guide Manufacturer Incident Report (MIR) (PDF, 360 kB, 20.11.2025)

01.12.2025

MU103_10_002e_FO Form PSUR/PBRER for human medicines (DOCX, 373 kB, 01.12.2025)

ZL000_00_021e_WL Guidance document Packaging for human medicinal products (PDF, 719 kB, 01.12.2025)

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