At Vital Signs Research Group, we bring precision and passion to the science of medical device testing. Specializing in the validation of non-significant risk devices, we help innovators move from concept to clearance—supporting FDA 510(k) submissions and product development with accuracy and integrity.

We follow ISO and FDA guidelines to rigorously test devices like:

• Cuffed and cuffless blood pressure monitors

• Pulse oximeters

• Heart rate and respiratory rate monitors

Whether you're preparing for regulatory submission or fine-tuning product performance, we’ve got you covered.

Looking for more? We also offer CRO services and clinical trial consulting, partnering with your team to ensure your device meets the highest standards—every step of the way.