TOXENTRA delivers toxicology, product safety and regulatory consulting for the pharmaceutical, medical device, cosmetic, chemical and nutraceutical industries.
Toxicology & regulatory consulting for pharma, medical devices, cosmetics, chemicals and nutraceuticals.
ERT-certified expertise supported by academic research and hands-on regulatory experience.
Global regulatory knowledge aligned with EMA, FDA, OECD, ISO and ICH frameworks.
Supporting clients across markets and jurisdictions with scientific rigor and integrity.
Decisions built on reliable data, structured risk assessment and sound scientific reasoning.
Objective, unbiased and confidential scientific consulting — free of commercial conflicts.
From early-stage safety evaluation to final regulatory approval, we bring science and compliance together at every step.
Scientific evaluation of the potential health risks associated with your products, from raw material to finished formulation.
Preparation and evaluation of safety documentation for cosmetic, chemical and nutraceutical products.
Supporting compliance with national and international regulations for pharmaceuticals, medical devices and related sectors.
Scientific and technical support throughout your product development lifecycle, from concept to submission.
TOXENTRA brings together toxicological assessment, product safety and regulatory strategy so your products reach the market safely and in full compliance. Our team works alongside R&D, quality and regulatory affairs teams across the pharmaceutical, medical device, cosmetic, chemical and nutraceutical industries.
Tell us about your product and regulatory pathway — our team will get back to you to schedule a consultation.
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