Basics of Medical Devices Regulatory Affairs
Our Basics courses on medical devices in the EU occur twice a year (in 2018 they were held in February in London and June in Ireland). This one-day course will give you a comprehensive overview of regulatory requirements and considerations for medical devices. Dates and locations for our 2019 events will be announced in early September 2018.
Medical Devices Regulatory Affairs Introductory Course
TOPRA delivers an annual three-day Introductory course in June for anyone new to Medical Device Regulatory Affairs looking to gain an in-depth understanding of the requirements for medical devices in the EU. The 2019 edition will be held on 10–12 July at a to-be-announced location in the UK. Registration for the event will open in early 2019.
We offer medical devices Masterclasses, aimed at experienced regulatory professionals through the year, including Drug-Device Combinations and Other Technologies on 3–5 September, and Regulatory and Related Activities in the Device Lifecycle on 24 October.
MSc Regulatory Affairs – Medical Devices
TOPRA's NEW MSc Regulatory Affairs (medical devices) is a qualification designed not only to help you broaden your regulatory expertise whilst developing your career, it is also fully flexible - designed to suit you so you can start when you want and pay as you go.
TOPRA Annual Symposium – Sweden
In 2018, TOPRA’s Annual Symposium will be in Stockholm between 1-3 October, with two days exclusively covering medical devices and IVDs. Find out what was discussed in previous years.