Essentials of In-Vitro diagnostics regulatory affairs

Master the fundamentals of IVDs with our ‘Essentials of In Vitro Diagnostics Regulatory Affairs’ training course. By giving you a comprehensive overview of the regulatory environment and the main processes and issues, it will provide you with the confidence to communicate the basics of IVDs in regulatory affairs.

By attending this training course on 3 July 2024 (in-person in London, UK or online), you will also:

🔹 Learn about main regulations and other controlling documents and how they can be applied to IVDs
🔹 Understand the key regulated markets and regulatory bodies for IVDs
🔹 Learn from expert speakers with practical knowledge and experience
🔹 Develop a network to support you for the rest of your career
🔹 Earn 6 CPD hours

This course is led by expert speakers from companies such as TÜV SÜD, IVDeology, Agilent Technologies and more, who have a combined wealth of knowledge and experience.

TOPRA members are eligible for discounted rates, as are professionals based in low-income countries (as defined by the World Bank), those working for regulatory or government agencies, academic institutions, charities, patient groups, or in full-time education.

Member: £395 +VAT*
Non-member: £395 +VAT*

Discounted places:
A limited number of discounted places are available at the rates below. Please email us at [email protected] for a discount code before making your booking.

Those working for regulatory agencies, government agencies or academic institutions: £296.25+VAT*
Those working for charities, patient groups or in full-time education: £197.50+VAT*
*VAT, if applicable, is charged at 20%