Date: Available on demand. Originally presented in June 2019.
Overview
The need for the Global Medical Device Nomenclature (GMDN) has never been greater, and is a mandatory data requirement in most regulatory jurisdictions. The webinar will give an insight into the GMDN and how the regulator affairs professional can best manage GMDN data.
Learning objectives
The aim of this webinar is to provide an understanding of:
-
The GMDN data structure
- The process for manufacturers
- GMDN and Unique Device Identification (UDI)
- Enhanced medical device data analysis using GMDN>Data quality/common misunderstandings
Target Audience
This webinar will appeal to Regulatory Affairs Professionals who are either involved or interested in Medical Devices.
Speaker
Edward Glenn is a term developer at the GMDN Agency responsible for drafting and management of GMDN terms; he is also focused on GMDN training for manufacturers, assisting hospitals, and improving data quality.
He joined the GMDN agency in 2012 after 10 years in the pharmaceutical industry as a medicinal chemist, working on small molecule drug projects in the fields of diabetic pain, antibiotics, HIV, and sleep/cognition therapy. Edward holds a Master’s degree in Chemistry from Oxford University.
CPD
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
How do I register?
Prices
| Type |
Member |
Non-member |
| Standard |
£70 + VAT |
£95 + VAT |
Discounted Places
A limited number of discounted places are available at the rates below for those:
Please email meetings@topra.org for a discount code before making your booking.
| Type |
Member |
Non-member |
| Discount |
£35 + VAT* |
£47.50 + VAT* |
* VAT, if applicable, is charged at a rate of 20%.
Terms and conditions
By purchasing this webinar, you are agreeing to the terms and conditions.