by Dr. Timo Weiland & Mirja Wild | Nov 27, 2024 | Advertorial, C3
The new version of the European regulatory framework for medical devices in the form of the MDR has resulted in a dynamization that affects existing medical devices as well as new products. The central elements “Clinical Evaluation Plan & Clinical...
by Lea Rebholz | Feb 7, 2023 | Advertorial, C3, Interviews
Clinical studies – that’s what the C3 in our 4C concept stands for. Our C3 also includes the clinical evaluation, a central process for medical device manufacturers and those who want to become one. We spoke to Robert Radloff, Director of Product...
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