We are excited to announce that RegDesk, the innovative Regulatory Information Management (RIM) platform, has been recognized as a Representative Vendor in the Gartner® Market Guide for Life Sciences Regulatory Information Management. Read the complimentary Market Guide for RIM Solutions report to learn more!
A Class 1 medical device is a type of medical device that poses a minimal potential for harm to the user and is generally considered to be low-risk.Class 1 medical devices include a wide range of products, such as bandages, crutches, elastic bandages, and orthopedic...
A class II medical device is a device that is intended to be used for a moderate-risk purpose. These devices may not pose the same level of risk as class III devices, but they still require some level of regulatory control to ensure their safety and effectiveness....
A medical device is a product that is used in the diagnosis, prevention, treatment, or management of a disease or medical condition. They are designed to assist healthcare professionals in their work and can range from simple instruments, such as a thermometer, to...
The new article addresses the aspects related to the design considerations for diagnostic clinical performance studies. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has...
RegDesk is recognized as a Regulatory Intelligence Representative Vendor! Learn more by reading the 2024 Gartner® Market Guide for Regulatory Intelligence Solutions.
Medical Devices
