Medical Devices
Toxway: Your Partner in Medical Device Safety and Compliance
Toxway provides expert biocompatibility services designed to ensure the safety and regulatory compliance of medical devices. Our comprehensive solutions help clients navigate the complexities of pharmaceutical and medical device regulations, focusing on international standards like EU MDR 2017/745, ISO 10993, and ISO 14971.
Our Sevices
Biological Evaluation Plan (BEP)
See MoreGap Analysis and Standard Gap Assessment
See MoreRisk-Based Biological Evaluation
See MoreToxicological Risk Assessment (TRA) of Extractables and Leachables
See MoreBiocompatibility Study Design & Monitoring
See MoreBiological Evaluation Report (BER)
See MoreRisk Management Plan (RMP)
See MoreChoose Toxway for Medical Device Biocompatibility Services to ensure your devices meet global safety and compliance standards with precision and expertise. Our team excels in aligning with EU MDR, ISO 10993, ISO 14971, and ISO 18562 standards, offering tailored solutions to address your unique project demands. Backed by a proven track record and deep industry knowledge, we navigate regulatory complexities with a client-centric approach, delivering personalized, flexible services that adapt to evolving needs. Trust Toxway as your dedicated partner in achieving biocompatibility excellence and advancing your medical device projects.