Swissmedic, Swiss Agency for Therapeutic Products
- Documents
- 50
- Date range
- 2016–2026
- Feb 1, 2016–Nov 1, 2026
- Languages
- 4
- Coverage
- 100%
- 49 of 49
- Last run
- 5 Nov 2026
Activity
Documents per year
Languages
Share of available renditions
- German27%
- English26%
- French24%
- Italian23%
Documents
50 documents
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
Guidance document RMP / ICH E2
Swissmedic MU103_10_001Aug 1, 2026EN
Guidance document Involvement of patient organisation in the review of Patient Information
Swissmedic ZL000_00_049Aug 1, 2026EN
Guidance document Authorisation of human medicinal product with known active pharmaceutical substance
Swissmedic ZL101_00_018Jul 15, 2026EN
Guidance document Authorisation of human medicinal product with new active substance
Swissmedic ZL101_00_005Jun 15, 2026EN
Guidance document Orphan Drug
Swissmedic ZL100_00_002Jun 1, 2026EN
Guidance document Project Orbis
Swissmedic ZL000_00_048Jun 1, 2026EN
Directory List countries with comparable control of human medicinal products
Swissmedic ZL000_00_011Jun 1, 2026EN
Guidance document Packaging for human medicinal products
Swissmedic ZL000_00_021Jun 1, 2026EN