Noah Labs is pleased to announce that we have achieved ISO 13485 certification as a medical device manufacturer. This is a testament to our commitment to quality and excellence in all of our product offerings.
The ISO 13485 is an international standard that specifies quality management system (QMS) requirements tailored to organizations involved in the design, development, manufacture, installation, and maintenance of medical devices and related services. A company must implement and maintain a quality management system that meets the requirements of the standard in order to be certified to ISO 13485.
For Noah Labs, this certification is not just a badge of honor; it is a testament to our dedication to providing world-class products and services in the healthcare industry, where safety, accuracy and reliability are critical. It demonstrates that our company has documented processes in place, follows best practices, and strives for continuous improvement.
This assures our patients that our quality management system maintains the highest standards for all of our services. We are pleased to have received this certification and are committed to providing you with the most advanced medical solutions to improve your quality of life.
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While it may seem overwhelming at first, this investment will provide you with significant benefits in the long run by serving as your ticket to the healthcare industry.
At Noah Labs, our mission is to help people with cardiovascular diseases live longer, healthier lives. With Noah Labs Ark, we have created an environment where a patient's health is independent of location and where intelligent algorithms detect deterioration early so that physicians can take timely countermeasures. We are developing software systems that understand, treat and ultimately prevent cardiovascular disease. Noah Labs is funded by EIT Health and the State of Berlin. We are also currently conducting clinical studies with Charité University Hospital in Berlin, UMC-Maastricht and Clinic Barcelona.