Regulatory Support:

EBRC provides an experienced support for all key phases of the evaluation and registration process for biocidal active substances and products:

• Annex I inclusion of active substances (both existing and new a.s.):
  Preparation of complete dossiers in support of Annex I inclusion of both new and existing active substances, including risk assessments, submission and defence of dossiers in the review process
  
  
• Data gap analysis and data package development as a prerequisite for a successful application
  
  
• Registration / authorisation of biocidal products:
  Preparation and submission of application dossiers for national registration / authorisation of biocidal products (i.e., Annex-II-B/III-B dossier, post Annex I inclusion)
  
  
• General services in the maintenance of regulatory approvals for products already on the market
  
  
• Planning, coordination and monitoring of experimental studies
  
  
• Task Force Management