Webinar: GMDN Primer for Regulatory Affairs Professionals

Webinar: GMDN Primer for Regulatory Affairs Professionals
Get an understanding of Global Medicinal Device Nomenclature (GMDN) and how this can be best managed.

: Wednesday 5 June 2019 
Time: 12:00 - 13:00 BST (GMT+1)


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.  


Edward GlennEdward 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.


This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.

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Course fees:
Type Member  Non-member 
Standard    £70+VAT £95+VAT 

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