Want to know how to keep your biocides on the EU market? Plan ahead with advice from our experts:

  • Learn strategies for dossier preparation, types of authorization, timelines, necessary documentation (IUCLID, PAR, SPC).
  • Be aware of dossier data requirements, intended uses, relevant exposure scenarios, proof of efficacy, risk assessment for humans and environment.
  • Understand the recent developments in ECHA guidance and manuals (e.g., dermal absorption, efficacy) which can impact your dossier preparation.

Presenters

  • Iryna Koval, PhD, Regulatory Affairs Manager, Charles River
  • Wendy van de Wiel MSc, Regulatory Affairs Manager, Charles River