At CEHTRA we are recognized for the strong dossiers we provide as we strive for a top quality service:
• We provide support at every stage of the process if requested, or just individual steps, including the Biological Evaluation Report by an ERT toxicologist.
According to the ISO 10 993 standard (part 1 to 20), Medical Devices have to comply to requirements related to Biological Medical Devices Assessment – a field where CEHTRA’s Toxicological Expertise and Expertise in Material Sciences will prove invaluable, especially for the risk analysis of Medical Devices:
• Physical & Chemical characterisation of Medical Devices
• Physical & Chemical characterisation of packaging materials
CEHTRA is a consultancy company specialised in chemical safety regulation.