Noah Labs is a digital cardiology start-up, based in Berlin and Boston. We already run a CE-marked remote patient... enrollment, and closing, on the sponsor side and without a full-service CRO Working knowledge of 21 CFR Parts 812, 50, 56 and 11...
deployed a CE-marked remote patient monitoring platform across Europe and is now advancing a voice-based Software as a Medical... enrollment, and closing, on the sponsor side and without a full-service CRO Working knowledge of 21 CFR Parts 812, 50, 56 and 11...
on holding ourselves to the highest standards of patient safety and product efficacy. Today, we are setting new standards... supervision Standards knowledge: ISO 13485, FDA 21 CFR 820.30, IEC 14971, IEC 62366, IEC 60601-1, IEC 60601-1-2 and collateral...
Noah Labs is a digital cardiology start-up, based in Berlin and Boston. We already run a CE-marked remote patient...-up through enrollment, and closing, on the sponsor side and without a full-service CRO Working knowledge of 21 CFR Parts...
Noah Labs is a digital cardiology start-up, based in Berlin and Boston. We already run a CE-marked remote patient...-up through enrollment, and closing, on the sponsor side and without a full-service CRO Working knowledge of 21 CFR Parts...
Frankfurt am Main (60318), Germany Posting date: 21 Aug 2026 Reference: 70590 Join a team dedicated to transforming the... offers an opportunity to make a meaningful impact on patient care while working in a collaborative and forward-thinking environment...
, EN). - Experience in sustaining regulated devices under Design Control (21 CFR 820), ISO13485, ISO14791, MDR and knowledge of applicable... and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the...
also responsible for integration of inputs and risks from multiple disciplines to ensure robust patient-centric product design... in combination product or medical device development and familiarity with FDA 21 CFR Part 820.30, 21 CFR Part 4, ISO14971, ISO 13485...
also responsible for integration of inputs and risks from multiple disciplines to ensure robust patient-centric product design... in combination product or medical device development and familiarity with FDA 21 CFR Part 820.30, 21 CFR Part 4, ISO14971, ISO 13485...
- one solution where researchers can simultaneously capture patient-reported and multimodal sensor data, from laboratory-grade... Collect's next chapter - deepening it for clinical research (RWD studies, cohort studies, patient registries, RCTs), enriching...