- Support
- Guidance
- Getting started
- Q&As Support
- Testing methods and alternatives
- Webinars
- Dossier Submission Tools
- Manuals
- REACH-IT
- Registration Process
- PPORD
- Notifying substances in articles
- Submitting downstream user notification of authorised uses
- Submitting a downstream user report for unsupported uses
- Submitting a downstream user report for classification differences
- How to submit and update your C&L notification
- Requesting an alternative chemical name in mixtures
- IUCLID
- CHESAR
- SPC Editor
- R4BP 3
- ePIC
- ECHA Cloud Services
- Validation Assistant
- Interact Portal
- EUSES
- National Helpdesks
- Practical examples of exposure scenarios
- Small and Medium-sized Enterprises (SMEs)
- Registration phases
- 1. Your registration obligations
- 2. Finding your co-registrants
- 3. Get organised with your co-registrants
- 4. What information you need
- Information requirements: 1 to 10 tonnes per year
- Information requirements: 10 to 100 tonnes per year
- Adaptations to the standard information requirements
- Information requirements: 100 to 1000 tonnes per year
- Information requirements: 1000 tonnes or above per year
- How to avoid unnecessary testing on animals
- Strategy for gathering your data
- 5. Creating your registration dossier
- 6. Submitting your registration dossier
- 7. How to get organised for dossier updates
- Practical examples of chemical safety reports
- Substance identification
- Authorisation
- Substances of very high concern identification
- How to apply for authorisation
- Are you affected by authorisation?
- Teleconference based information sessions - terms and conditions of use
- Develop an application strategy
- Submission windows
- Start preparing your application
- Teleconference Based Information Sessions
- Formats for applications for authorisation
- Notify ECHA and request a teleconference based information session
- Previous events on appliction for authorisation
- Finalise your application
- Partners service for applicants
- Submit your application
- Engage during the opinion development
- Ask ECHA about authorisation applications
- Fulfil your obligations
- Evaluating applications
- Information on applying for authorisation by Member States and industry organisations
- Submit a review report if you still need to use the substance
- Restriction
- Submission of CLH dossiers
- Socio-economic analysis in REACH
- QSAR Toolbox
- Mixture classification
- UK withdrawal from the EU
- Know your role
- UK-company based in Northern Ireland
- UK-based REACH registrant
- UK-based only representative
- UK-based manufacturer or supplier under the BPR
- EU-based company
- UK-based mixture supplier
- UK-based authorisation holder under REACH
- EU downstream user of an authorised substance
- Manufacturer or formulator outside the EU/EEA
- Advice to companies
- Procurement and contracts
- Know your role
- Recommendations to registrants
- ECHA accounts and EU Login
- Technical completeness check
National Helpdesks
National helpdesks have been established as the first point of contact for questions related to the BPR, CLP and REACH regulations. They can give you advice in your own language and are aware of local conditions that can be relevant for the correct compliance with these regulations. You can find their contact details below.
Czech Republic
- BPR competent authority
- Ministry of Health of the Czech Republic
Palackeho namesti 4 CZ - 128 01 Prague 2
Telephone: +420 267 082 305
Fax: +420 267 082 228
Email: biocidy (at) mzcr.cz
BPR website - CLP and REACH helpdesk
- CENIA Vrsovicka 1442/65, 100 10 Prague 10
Telephone: +420 267 125 323
Email CLP: clp (at) cenia.cz
Email REACH: reach (at) cenia.cz ;
REACH website
CLP website
Route: .live1
