Prerequisites: first, you must have followed this course > Implementing GS1 standards for medical devices (UDI) and in vitro medical devices (IVDR) or follow this learningplan on My Training.
Duration: 2 hours
The standardised product sheet follows your products from production to delivery to pharmacies, hospitals, ..... It allows you to register and exchange your product data (commercial, regulatory, marketing or logistics) in real time with all your commercial partners.
Want to market your products faster and easier? Reduce distribution costs, improve the quality of your data and simplify compliance with standards and regulations?
Thanks to our My Product Manager platform and related applications, you will learn how to share and register your Basic-DI, UDI-DI and legacy devices in EUDAMED.
Programme:
- Manage and synchronise product data.
- Understand the need for product information.
- Learning how to complete the GS1 product data sheet.
- Gain understanding of how My Product Manager works and the data management tools.
- Using the My UDI Manager applications.
- How to send data to the FDA and EUDAMED.
- Manual and fast creation of product sheets via mass import of products in the My Product Manager Share interface for medical devices and for Belgian and Luxembourg data recipients.
- Gain more information about the fields to be filled in based on the ECHO Data Model.
After the training, a participation certificate will be issued upon request.
The dates and times do not suit you? Take a look at our tailor-made trainings
Questions? Contact us via support@gs1belu.org
This course is subject to our cancellation policy.
Practical information
Type:
Webinar/Virtual training
Location:
Webinar URL
Access:
GS1-members: Included in the membership
Non-members: € 75