This webinar will provide clarification on which medical device facility or establishment must register and list, how to register and list, and how to coordinate the payment process to accomplish the actual registration or device listing.
During this 60-minute webinar, the speaker will provide key information and practical knowledge that will help you to sort through the confusion and have your medical device facility or establishment registered and product listed.
Why Should You Attend:
There is no current guidance available on device registration and listing. Though there is much information on the FDA website about who must register and list, how to register and list, it can all still be a bit confusing to coordinate the payment process with accomplishing the actual registration or device listing.During this 60-minute webinar, the speaker will provide key information and practical knowledge that will help you to sort through the confusion and have your medical device facility or establishment registered and product listed.
Areas Covered in the Webinar:
- Background of the device registration and listing
- How does registration and listing relate to MDUFMA?
- What is FURLS?
- Who must register and list?
- When are you required to register and list?
- How do you register and list?
- How do you pay your annual fee for registration?v
- Do you need a US Agent? If so, what are the responsibilities of the agent?
Who Will Benefit:
This webinar will provide valuable assistance to following personnel in the medical device industry:- Regulatory affairs
- Project managers
- Staff involved with regulatory filings
- Product Development managers
- Documentation
- Senior Management
- Finance
Course Provider
Cheryl Wagoner,
