Precision Testing. FDA-Ready Results.
At Vital Signs Research Group, we bring precision and passion to medical device testing. Based in San Francisco, we specialize in validating non-significant risk devices and supporting FDA 510(k) submissions with accuracy and integrity — helping innovators move from concept to clearance.
We follow ISO and FDA guidelines to rigorously test the devices that monitor the vital signs people depend on every day. Our studies are designed to meet current regulatory standards at every stage — whether you’re refining a prototype or preparing your final submission package.
We test a full range of noninvasive vital signs devices, including cuffed and cuffless blood pressure monitors, pulse oximeters, heart rate and respiratory rate monitors, clinical thermometers, and glucometers.
We also offer CRO services and clinical trial consulting, partnering directly with your team to navigate protocol design, IRB approval, and participant recruitment. Whatever stage you’re at, we’ve got you covered.
Ready to get started? Reach out to our team today — let’s turn your innovation into impact, one data point at a time.
