Obligations to the manufacturers of chemicals
- Self-regulation
- Objects
- Product register for chemicals
- Substances
- Obligation to report preparations
- 1. Purpose of reporting
- 2. Who is required to submit reports?
- 3. When must a report be submitted?
- 4. Which substances and preparations have to be reported?
- 5. What information on substances and preparations has to be reported?
- 6. In what format are reports to be submitted?
- 7. When does a report need to be updated or a new UFI generated?
- Simplification of the registration application procedure for preparations
- Voluntary reporting of a preparation in the Chemicals Product Register (RPC)
- Remarks concerning the notification of a preparation with labelling EUH208
- Authorisation biocidal products
- Biocidal active substances
- Transitional authorisations (AN/AC)
- Product types
- Authorisations according to the European harmonized system
- Questions on delimitation
- Treated articles
- Swiss specific authorisation provisions
- Declaration requirements for quantities of biocidal products placed on the market
- Registration application of a parallel imported plant protection product