Toxentra provides end-to-end toxicology and regulatory services that support product safety, compliance and market access across global markets.
Comprehensive risk assessments to protect human health and support regulatory compliance.
Learn MoreBiological evaluation and biocompatibility services in accordance with ISO 10993 standards.
Learn MoreSafety evaluation and regulatory support throughout the medical device lifecycle.
Learn MoreScientific safety assessment and report preparation in line with EU Cosmetics Regulation (EC) No 1223/2009.
Learn MoreEvaluation of clinical, pharmacological and biopharmaceutical data to support product development and regulatory submissions.
Learn MoreIn silico solutions including CADD, small molecule design, metabolite synthesis, QSAR, docking and predictive toxicology.
Learn MoreStrategic regulatory advice and scientific solutions tailored to your product and target markets.
Learn MoreTailored training programs and workshops on toxicology, pharmacovigilance and regulatory sciences.
Learn MoreFrom early development to regulatory approval, Toxentra provides tailored scientific solutions for every stage of your product lifecycle.
We learn about your product, goals and regulatory needs.
Our experts conduct the necessary evaluations and studies.
We develop a clear strategy to meet regulatory requirements.
We deliver comprehensive reports and continue to support you.
