The products Nectar develops must be trusted to improve, and sometimes even save, patient’s lives. Thus the creation of products must be finely tuned, requiring tedious and detailed assessment; an ISO 13485 certified QMS is proven to support this undertaking.
For Nectar, being ISO 13485 certified goes beyond holding this highly qualified certificate. Our medical device quality assurance has been woven into our DNA as regulatory compliance standards can be found through each step of our proven process. From research to verification, Nectar’s quality engineers track and record every single variable to ensure our medical devices and products are safe and reliable.
For our clients and consumers, our ISO 13485 medical device certification and quality assurance system can assure that your medical devices and software systems are achieving the most prestigious standards possible in the global market.