Our programme is shaped by members, not by committee. These are the areas RTP is currently developing working groups and conference sessions around.
New Approach Methodologies - Read-across - QSARs - AI in Toxicology - Weight of Evidence
REACH & CLP - Biocides & Plant Protection Products - Pharmaceuticals - Food Contact Materials & Additives - Cosmetics - Emerging Regulatory Frameworks
Genotoxicity - Mutagenicity - Carcinogenicity - Reproductive & Developmental Toxicology - Endocrine Disruptors - Sensitisation - Nanomaterials
Harmonisation between EU, UK post-Brexit, US EPA, TSCA, China REACH, and Korea K-REACH and other international frameworks — reducing duplication while maintaining safety standards.
Dose-response modelling - Toxicokinetics - Cumulative Risk assessment - Mixture Toxicology - Emerging regulatory approaches to combined exposure and the 'chemical cocktail' problem
Practical guidance on building compliant registration dossiers using IUCLID and ECHA submission portals, including navigating SVHC identification and Annex XIV/XVII processes.
Tracking emerging and upcoming legislation across jurisdictions to help organizations anticipate regulatory change and plan compliance strategies proactively.
Real-world regulatory dossiers and worked examples illustrating practical application of hazard and risk assessment methodologies across sectors.
Structured learning pathways - Continuing professional development content - Build and maintain regulatory toxicology expertise - Access to a network of regulatory toxicology experts for consultations and peer discussion