Highlights
Regulatory Aspects
You will meet authorities, such as directors, heads, managers and consultants of:
Regulatory Aspects
- Maximum residue levels: Legislation on limits for residues of active substances in biocidal products
- Dossier preparation for in situ generated active substances under BPR requirements
- Industry perspective on union authorisation
- Specific regulatory changes in the ‘same biocidal product’ regulation
- Obligations in the supply chain: Enforcements in the biocidal market
- Industry perspective on product families: Practical examples
- Product families: Recommendations from a regulatory point of view
- Availability of nanobiocides and treated articles in the EU and challenges in implementing the BPR
- New guidance on disinfection products
- Industry perspective on future challenges with disinfectants and disinfectant by-products under the BPR
You will meet authorities, such as directors, heads, managers and consultants of:
- Legal and Regulatory Affairs
- Registration and Authorisation
- Research and Development
- Product Safety
- Product Management
- Regulatory Science
- Chemical and biocides industry
- Producers of biocidal products
- Industrial and professional users of biocides
- Research institutes
- Regulatory Authorities
- Environmental and health risk consultants
- Professional associations