We offer companies a specialized service for preparing Biological Evaluation Plans and Reports according to MDR and ISO10993-1:2025 requirements.
Your project will be overseen by a dedicated project leader, backed by a regulatory affairs expert, who will personally handle your consultation needs. They’ll collaborate closely with a qualified toxicologist to ensure comprehensive support.
Our service is invaluable for companies seeking to guarantee the biological safety of their medical devices. With our team of specialized experts, you’ll have the specific knowledge and skills required to conduct these evaluations effectively.
