When: 3 - 5 June 2025
Where: Online
Day 1 start time: 09:00 GMT Day 3 end time: 16:30 GMT
Also available as a face-to-face course, please click here for the face-to-face registration option
Course overview
This Masterclass will cover:
- US FD&C Act and Code of Federal Regulations
- History, Structure and Mission of the FDA
- Product Designation and Device Classification
- Pre-Submissions, Pre-Market Notification & Approval
- Combination Products
- Device Listing and Establishment Registration
- Labelling
- Quality Systems Regulation and Inspections
- Medical Device Reporting
Benefits to delegates
This course will enable you to:
- Understand the global importance of the US medical devices market and the history and context of medical device regulation in the US
- Demonstrate a critical understanding of the US medical devices regulation, processes and procedures
- Critically evaluate the different routes into the US medical device market and the regulatory requirements and processes for each
- Evaluate the differences and similarities between the regulation of medical devices in the US and EU
- Be able to make recommendations about entering the US medical devices market and a suitable strategy for doing so. This will include the ability to apply product jurisdiction, device classification criteria and identify relevant regulatory pathways and requirements
- Make sound judgments in he absence of complete data and communicate their conclusions effectively
- Critically appraise and evaluate communications relating to medical devices from US regulatory bodies and research publications
CPD: This course provides 15 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Programme
You can view and download an example programme based on previous courses here
Module Leader
Presenter
TOPRA Masterclasses are developed and delivered by a
faculty of expert speakers from relevant industry, agencies, notified bodies
and other stakeholders, and are validated by the University of Hertfordshire.
In addition to the module leader(s) listed above, confirmed speakers for this
course include:
Suitable for
- Delegates from the regulatory affairs industry who wish to develop their knowledge of the requirements of medical devices in the US market
- Delegates from allied industries who wish to have a comprehensive understanding of the subject
Pricing
Standard
Type
TOPRA Member: £1900 plus VAT*
Non Member: £2100 plus VAT*
* VAT, if applicable, is charged at the rate of 20%
Discounted places
- Those working for regulatory agencies, government agencies or academic institutions
- Those working for charities, patient groups or in full-time education
A limited number of discounted places are available. Please note that discounted places are not valid for those enrolled on the MSc course.
Please email us at meetings@topra.org for a discount code before making your booking.
Terms and conditions
By booking a place on this course you are agreeing to the training terms and conditions.