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Topics
- Biocidal products in agriculture
- Brexit
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- Coronavirus COVID-19
- Endocrine disruption Biocidal products
- Grace periods
- Green Deal
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- Laws and regulations
- Low-risk products
- Manuals assessment framework
- Neonicotinoids
- Outdoor use of rodenticides
- Plant protection products and local residents
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Plant protection products
- Application process
- Pre Application Support
- Intake phase
- How to apply?
- Assessment framework
- Registration Manual
- Evaluation Manuals
- Evaluation Manual Biopesticides
- Explanation Guidances
- Methods
- Types of application
- Procedure zonal application
- Netherlands Rapporteur Member State Zonal Application
- Netherlands Concerned Member State Zonal Application
- Application for mutual recognition
- Comparative assessment
- Product Renewals (NL zRMS and NL=CMS)
- Change product authorisation - major changes
- Minor or administrative changes
- Minor change to legal instructions for use (WG/WGGA)
- Minor uses
- Procedure for national extension of authorisation with minor uses solely in the Netherlands (NLKUG)
- Parallel trade permit
- Derived trade permit
- Transitional legislation re-registrations under the Regulation
- Export certificate
- Request for information vertebrates testing
- Exemption for trial purposes
- Derogation for an emergency situation
- Adjuvants for plant protection products
- Withdrawal of authorisation or permit
- Application for active substance
- New active substance approval
- Renewal of active substance approval
- Ctgb policy for products containing pheromones and attractants
- Application for setting Maximum Residue Limit
- Characteristics
- Registration process & instructions for submission
- Evaluation of substances (other)
- Reporting new information on authorisation
- Immediate notification by the authorisation holder
- Annual notification by the authorisation holder
- Tariffs
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Biocides
- Application process
- Which procedure should I follow?
- Specific biocidal products
- Directions for submission biociden
- Pre Application Support
- Intake phase
- Grace period biocidal products
- How to apply?
- Application under regulation
- National product authorisations (BPR)
- Union Authorisations
- Re-registration and renewals
- Mutual recognition
- Major changes on request
- Minor, administrative amendments and withdrawal
- Simplified authorisations products containing low risk substances
- Same biocidal product
- Trial permit and notification
- Export certificate
- Request for information on animal testing
- Application under transitional legislation
- Limited assessment procedure
- Full assessment procedure
- Parallel trade permit
- Derived trade permit
- Minor and administrative changes under Transitional legislation
- Frame formulations
- Trial permit and notification
- Export certificate
- Request for information on animal testing
- Derogation Biocides for an emergency situation
- Application active substances
- Approval active substances
- Renewal active substances
- Assessment of equivalence of active substances or additive
- Substances of Concern
- Comparative assessment for products containing a candidate for substitution
- Assessment framework and manuals
- Registration Manual
- Evaluation Manual
- Explanation guidance
- Immediate notification potentially harmful or unacceptable effects
- Tariffs
- About the Ctgb
- Overview of authorisations