Pharmaceutical Environmental Risk Assessment & Regulatory Toxicology
ToxWriter provides Environmental Risk Assessment and regulatory toxicology support for pharmaceutical products, with a focus on EU and UK requirements.
Explore ReportsRequest a ReportSpecialised toxicology and regulatory safety support
Whether the product is a drug, medical device, cosmetic, consumer product, or food ingredient, ToxWriter provides scientific toxicological risk-assessment and regulatory support to help clients address product-safety requirements and prepare for technical and regulatory review.
Environmental Risk Assessment
Phase I exposure assessment, Phase II fate and effects evaluation, data gaps, testing strategy, PEC/PNEC considerations and regulatory-ready reporting.
Regulatory Toxicology
ICH M7, impurity assessment, genotoxicity, QSAR, PDE/ADE, OEL, OEB and OHC support.
Scientific Writing and Product Safety
CTD/eCTD writing, cosmetics safety, biocompatibility and extractables and leachables assessment.