Swissmedic, Swiss Agency for Therapeutic Products
- Documents
- 50
- Date range
- 2016–2026
- Feb 1, 2016–Sep 7, 2026
- Languages
- 4
- Coverage
- 100%
- 49 of 49
- Last run
- Sep 18, 2026
Activity
Documents per year
Languages
Share of available renditions
- German27%
- English26%
- French24%
- Italian23%
Other sources
Confederation
- Federal Supreme Court178'338
- Federal Administrative Court93'350
- Official Bulletin70'306
- Parliamentary business67'727
- Federal Supreme Court Official Reports35'388
- Official Compilation of Federal Legislation23'144
- Federal Gazette11'986
- Federal Criminal Court11'127
- Federal Administrative Authorities Case Law10'965
- Systematic Compilation of Federal Legislation6'363
- Federal Social Insurance Office (FSIO)2'281
- Swiss Private Insurance Law Court Judgments (published by FINMA)2'233
Documents
50 documents
Guidance document GMP compliance by foreign manufacturers
Swissmedic ZL000_00_036Sep 7, 2026EN
Guidance document Renewal and discontinuation of authorisation or change of status (main authorisation/export licence)
Swissmedic ZL201_00_001Sep 1, 2026EN
Guidance document Authorisation of individual teas, cough and throat lozenges and pastilles in the notification procedure HMV4
Swissmedic ZL103_00_003Sep 1, 2026EN
Guidance document Formal requirements
Swissmedic ZL000_00_020Sep 1, 2026EN
Liste pays dont le système de contrôle des BPF
Swissmedic BW105_00_002 variant bw105_00_002f_vzlistedespaysdontlesystemedecontroledesbpfAug 12, 2026FR
List Countries with recognised GMP control systems
Swissmedic BW105_00_002Aug 12, 2026EN
Guidance document Mobile technologies
Swissmedic ZL000_00_050Aug 1, 2026EN
Guidance document Maintenance and updating of Annex 1
Swissmedic ZL000_00_042Aug 1, 2026EN
Guidance document Minimising the risk of TSE
Swissmedic ZL000_00_035Aug 1, 2026EN
Guidance document Authorisation of allergen product
Swissmedic ZL000_00_032Aug 1, 2026EN