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
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- 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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