Toxicological Risk Assessment – TRA

Toxicological Risk Assessment TRA

One topic in which we are experts here at ToxHub are Toxicological Risk Assessment (TRA) for medical devices, conducted according to ISO 10993-17!

For short, a TRA it’s an assessment of product safety, conducted taking into account its composition and intended purposes. This evaluation can be done only by board-certified toxicologists, like our Carla Landolfi, who is an European Registered Toxicologist (ERT) with more than 25 years of experience in toxicology – both regulatory, in vitro and in vivo.

🤝With our client-centered consultancy approach, we prioritize meeting your needs while ensuring adherence to the highest safety standards.

✨ Your satisfaction is our top priority!

📩 Contact us for a quote and discover how we can support your medical device needs!




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Do you need a TRA for your products? Contact us!