Karin Nydahl Laboratorieingenjör Tel +46 10 516 59 28 Email karin.nydahl@ri.se Location Borås Ask me about Posts Ask me about Service ISO 10993-5 Cytotoxicity Test - in vitro Cytotoxicity testing is a crucial part of the biological evaluation of medical devices and is a necessary step to meet the requirements of the Medical Device Regulation (MDR). RISE conducts cytotoxicity testing according to ISO 10… Service ISO 10993-23 Skin Irritation - in vitro Irritation testing is a critical component of the biological evaluation of medical devices and a necessary step to meet the requirements of the Medical Device Regulation (MDR). RISE conducts irritation tests according to ISO 10993… Posts 2025-02-24 / Karin Nydahl Biocompatibility testing: How collaboration makes a difference Ensuring biocompatibility in medical devices is complex and requires careful planning, collaboration, and adaptability. In this interview, Cecilia Wikell from Cochlear shares insights on the challenges of biocompatibility testing … 2025-02-18 / Karin Nydahl Navigating biocompatibility regulations in medtech In the medical device manufacturing field, ensuring biocompatibility is crucial. Regulatory requirements are stringent and vary by market and device use, making compliance complex. Karin Nydahl, laboratory engineer at RISE, shares…