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Karin Nydahl

Laboratorieingenjör

Tel
+46 10 516 59 28
Email
karin.nydahl@ri.se
Location
Borås
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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…
Expertise

Sustainability in healthcare products

The healthcare sector accounts for 4.4% of global greenhouse gas emissions. If it was a country, it would be among the five largest emitters. When there is a need to develop sustainable products and packaging for healthcare, RISE …
Posts
Biocompatibility testing: How collaboration makes a difference
2025-02-24
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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 …
Navigating biocompatibility regulations in medtech
2025-02-18
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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…