Date: Available on demand. (Original presentation date: June 2019)
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.
- 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
This webinar will appeal to Regulatory Affairs Professionals who are either involved or interested in Medical Devices.
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.
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
Once you have purchased the webinar, you will receive an email from firstname.lastname@example.org with a link to the webinar within one hour. Once received, simply click on the link in the email to access the webinar. You will have access to the webinar for six months from the day of purchase.
Please note, if you select the pay later option, you will not have access until payment has been cleared.
Terms and conditions
Please read the training terms and conditions before booking this webinar. By booking this webinar, you are agreeing to the terms and conditions.
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