NRSign – Advancing Healthcare Innovation
NRSign specializes in the design, development, and manufacturing of investigational and research medical devices, ensuring compliance with the highest industry standards.
Our Expertise
🔹 Regulatory Affairs – Preparation and submission of IDE, 510(k), PMA, ITA, and Health Canada approvals, along with post-market surveillance and compliance support.
🔹 Clinical Trial Support – Strategic guidance in clinical trial design and execution to validate the safety and efficacy of investigational devices.
🔹 Quality Management Systems (QMS) & ISO Certification – Assisting organizations in implementing QMS and achieving ISO certification readiness.
Why Choose NRSign?
With a multidisciplinary team of engineers, regulatory specialists, and quality assurance experts, NRSign is dedicated to advancing medical innovation through precision, compliance, and excellence.
GENERAL ENQURIES
OFFICE HOURS
| Monday – Firday | 8:00 – 5:00 |
| Saturday | 9:00 – 5:00 |
| Sunday | 11:00 – 4:00 |