The information supplied with medical devices, both on their labels and in any accompanying instructions for use form part of the device itself, and are critical to the safety and performance of the device and to compliance with regulatory requirements. This course provides an introduction to the regulatory requirements as they relate to the labelling of medical devices and how manufacturers may demonstrate compliance.

Organiser: Management Forum

Location: Virtual

Contact: https://ipi.academy/product/details/2695/unique-device-identification-udi-and-labelling-for-medical-device-manufacturers