Swissmedic, Swiss Agency for Therapeutic Products
- Documents
- 50
- Date range
- 2016–2026
- Feb 1, 2016–Oct 1, 2026
- Languages
- 4
- Coverage
- 100%
- 49 of 49
- Last run
- Oct 13, 2026
Activity
Documents per year
Languages
Share of available renditions
- German27%
- English26%
- French24%
- Italian23%
Other sources
Confederation
- Federal Supreme Court178'669
- Federal Administrative Court93'698
- Official Bulletin71'147
- Parliamentary business68'473
- Federal Supreme Court Official Reports35'393
- Official Compilation of Federal Legislation23'195
- Federal Gazette12'012
- Federal Criminal Court11'174
- Federal Administrative Authorities Case Law10'965
- Systematic Compilation of Federal Legislation6'370
- IPI trademark opposition decisions4'351
- Federal Social Insurance Office (FSIO)2'296
Documents
50 documents
Guidance document Import of a human medicinal product according to Art. 14 para. 2 and 3 TPA (parallel import)
Swissmedic ZL106_00_888Oct 1, 2026EN
Guidance document Authorisation biosimilar
Swissmedic ZL101_00_012Oct 1, 2026EN
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 efe263Aug 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