TOXENTRA provides scientific and toxicology services supporting product safety and evidence-based decision-making across different stages of product development.
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 and biological evaluation 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 MoreScientific solutions tailored to your product and target markets, aligned with regulatory requirements.
Learn MoreTailored training programs and workshops on toxicology, pharmacovigilance and product safety.
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 scientific needs.
We conduct the relevant scientific evaluations and identify appropriate assessment needs.
We provide scientific solutions aligned with applicable regulatory requirements.
We deliver comprehensive reports and continue to support you.
