Led by expert speakers from industry and regulatory agencies, this three-day training course will cover all aspects of the product development process, offering you a comprehensive understanding of EU legislation and regulatory procedures.
Taking place between 15-17 April 2025 in-person in London, UK, you will also learn about the central role regulatory affairs plays in healthcare companies and the development cycle of new drugs.
This course is ideal for those who are new to regulatory affairs and looking for a comprehensive understanding of the pharmaceuticals industry, as well as established professionals looking to refresh and expand their knowledge.
By attending this course, you will:
✅ Gain the practical skills you need to become a highly effective regulatory affairs professional
✅ Take part in four interactive days with a comprehensive range of topics and case studies
✅ Develop a network to support you for the rest of your career
✅ Learn from expert speakers with practical knowledge and experience
✅ Earn 30 CPD hours
This course is Module 0 in our MSc programme developed and delivered by a faculty of expert speakers and validated by the University of Hertfordshire.
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.
