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GAB Consulting offers the full range of services required for the registration of your biocidal active substances and products in Europe according to Directive 98/8/EC and related review regulations. Rely on the support of our biocidal group experts from the initial check of available data to the final approval of your biocidal products.

Contact:
Kerstin Schrade
Dr. Joachim Rumbolz
  • Dossiers for the EU evaluation of active substances
  • National registration of biocidal products in accordance with Directive 98/8/EC
  • Dossiers in OECD format or according to the current TNsG
  • Check of completeness for available data sets
  • Preliminary risk assessments in toxicology, environmental fate and ecotoxicology
  • Expert statements in toxicology, environmental fate and ecotoxicology
  • Modelling and development of exposure scenarios
  • Stand-alone risk and exposure assessments in accordance with the relevant TGD
  • Support in contracting experimental work (studies)
  • Study monitoring
  • Compilation of IUCLID data sets
  • Expert discussion with authorities
  • Contacts to registration authorities within EU and Eastern European countries
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