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Topics

• Obligations to the manufacturers of chemicals
  • Self-regulation
    • Classification
    • Packaging
    • Labelling
      • Derogations from the labelling
      • Use of an alternative chemical name
      • Hazard pictogram
      • UFI (Unique Formula Identifier)
        • UFIs for biocidal products
    • Safety Data Sheet (SDS)
    • Advertising
    • Restrictions and interdictions
    • Obligations according the Nagoya ordinance
  • Objects
  • Product register for chemicals
    • Future development of RPC
      • News
      • Release Notes
    • User accounts
      • Principle of linking and administrative processes
      • User roles
      • Migration of the existing roles
      • Opening and managing user accounts
      • User management by the main users
      • Authorship
      • Sharing or replacing information protected by the authorship
      • CH-Login: Mutation of the user account
      • Two-factor authentication
    • Information on the entry/maintenance of products in the RPC
      • Product status
      • Product duplication function
      • Information for entering the composition
        • When is an ingredient declared?
        • Simplifying the notification process for preparations
      • Transfers and mutations
      • Training materials (RPC)
    • Mass reporting interface (MMT)
  • Substances
    • New substance
      • Electronic delivery of authorisation
      • Requirement to notify
      • New substances in a nutshell
      • Exemptions to the requirement to notify substances
      • IUCLID
      • Reporting of new substances that are exempt from the obligation to notify
    • Existing substance
      • Obligation to report substances
    • Candidate list of Substances of very high Concern (SVHC)
    • Substances in Annex 1.17 ORRChem (Annex XIV REACH)
      • Practical information
      • FAQ – Frequently asked questions
      • Reporting pursuant to number 3
      • Current consultations on requested uses
      • Past consultations on requested uses
      • Public Register of approvals pursuant to paragraph 4 number 2 Annex 1.17 ORRChem
    • Intermediate
  • 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
      • article 95 (of the EU biocidal product regulation, BPR)
      • In situ active substance from precursor
      • ECHA public consultation on potential candidates for substitution and on derogations conditions
    • Transitional authorisations (AN/AC)
      • Electronic delivery of authorisation
      • Simplified examination AN
      • Authorisation AN
        • Authorisation AN procedure for disinfectants
          • Comments on the legal situation regarding disinfectants
            • Overview of the legal basis and authorities with which disinfectants must be authorised in Switzerland
          • Efficacy dossier
          • Disinfectant active substances
          • Disinfectants with required efficacy dossier
          • Explanations for the testing and the evaluation of chemical disinfectants
        • Wood preservatives
        • Authorisation procedure AN for in situ generated active substances
      • Authorisation AC
      • Authorisation of same products AN/AC
        • The applicant is identical with the holder of the authorisation for the reference product
        • The applicant is not identical with the holder of the authorisation for the reference product
      • Authorisation of a biocidal product family AN/AC
        • Authorisation AN procedure for disinfectants
        • Wood preservatives
        • Authorisation procedure AN for in situ generated active substances
      • Application for authorisation for parallel trade AN
      • Changes to existing authorisations AN
      • Transitional provisions
    • Product types
    • Authorisations according to the European harmonized system
      • Authorisation AL
      • Recognition in parallel
      • Mutual recognition in sequence
      • Simplified authorisation
        • Notification of a simplified authorisation
      • Union authorisation
      • Authorisation for parallel trade
      • Authorisaion for a same biocidal products
      • Authorisation of a biocidal product family
      • Changes to existing authorisations
      • Extension of existing authorisations
    • Questions on delimitation
      • Cosmetics
      • Products for animals
      • Permethrin-containing topical insecticides
    • Treated articles
    • Swiss specific authorisation provisions
      • Algae and moss
      • New authorization requirements for rodenticides with anticoagulants
      • Authorisation for the disinfection of drinking water
      • Use of chemical air disinfectants prohibited when persons are present
    • Declaration requirements for quantities of biocidal products placed on the market
  • Registration application of a parallel imported plant protection product
• Obligations to the importers of chemicals
• Forms
• Obligations when using chemicals
  • Special Licences
  • Offers for training and further education
• Obligations in regard to the supply of chemicals
  • Specialist knowledge for chemical sales
  • Chemicals contact person
• Export to EU: REACH Helpdesk and CLP Helpdesk
  • REACH Helpdesk
    • REACH principles
    • REACH registration
      • Dossier requirements
      • Inquiry
    • REACH Restriction
    • REACH Authorisation
    • REACH and Switzerland
    • Substances in articles (products)
      • Articles with substances of very high concern: duty to provide information
      • Articles with substances of very high concern: obligation to notify
      • SCIP: database with information on articles containing SVHCs
      • Switzerland
  • CLP information
    • CH Exporters: Classification and Labelling - Notification pursuant to CLP
      • Who has to notify a substance to the CLP-inventory?
      • Which substances have to be notified?
      • What must be notified in accordance with Art. 40 (1) CLP?
      • How to notify
    • CH Exporters: Poison centre notification pursuant to CLP
• Good Laboratory Practice (GLP)
  • GLP Compliance Monitoring Programme
  • GLP-Test Facilities
  • Service Providers
  • GLP-interpretations / Newsletter
  • AGIT
  • GLP authorities
  • Animal experimentation
  • Request application to be listed in the GLP Register
• Chemicals Legislation and Guidelines
  • Chemicals Legislation
    • Chemicals Ordinance (ChemO)
    • Ordinance on Biocidal Products (OBP)
      • Annex 1, OBP
      • Annex 2, OBP
      • MRA Switzerland-EU
    • Chemical Risk Reduction Ordinance (ORRChem)
    • Strategy for Chemical Safety
  • Adaptations Chemicals Legislation
  • Status of the harmonisation of Swiss Chemicals legislation with international regulations
    • ATP in the CLP Regulation
  • Guidelines and Interpretation Aids to the Chemicals Legislation
    • Information Sheets
    • Alternative Test Methods
    • Washing and cleaning agents
    • RIVM Exposure assessment
    • Reports and Publications
  • Market control
    • Campaigns regarding chemicals

Product register for chemicals (RPC)

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