Areas of expertise.
Toxicology, Pharmacology, and Regulatory Compliance
With over 25 years of combined experience in toxicology, pharmacology, and regulatory affairs, the ToxHub team brings extensive expertise across Medical Devices, Pharmaceuticals, Cosmetics and Chemicals industries.
Biological Evaluations of Medical Devices
Expertise in Combination Products and Substance-Based Devices
Expertise in both Small Molecules and Peptides, from early stage to post-market product safety.
Excellence in Impurity Characterization, Occupational Exposure Limits (OELs) and Environmental Risk Assessment (ERA)
Expertise in Toxicological Characterization of New Cosmetic Ingredients, including Botanicals and Nanomaterials
Industry Chemicals and Biocides
Expert support for REACH, CLP, and BPR Compliance
More than just an answer
Personalized guidance and close dialogue.
Support through the entire regulatory process.
Profound knowledge in both toxicology and pharmacology.
Leading drug manufacturer in Central and Eastern Europe
“Thanks again for the excellent work! Brilliant quality of the reports, timely delivery, and great customer contact. I am very happy with our collaboration and am looking forward to the next projects!”
Complementary documentation of missing ADME data to respond to the notified body | Eye Drops
Global pharmaceutical company
“On behalf of my Company I just wanted to share our sincere thanks for your excellent work on the report.”
Report on non-genotoxic impurity qualification | Therapeutic Proteins
European medium-sized MedTech company
“I take this opportunity to thank you for your professionalism and availability. Hearing the experiences of other companies, I can tell you that what you do is not a given.”
Biological Evaluation Reports (BER) | Substance-based Medical Devices
Years of experiences from the Pharma and Biotech Industry
Substances evaluated
Biocompatibility Testing Programs approved by EU Notified Bodies
Toxicological Risk Assessment reports delivered
